LEONA e.V. - Familienselbsthilfe bei seltenen chromosomalen Veränderungen
     Note relative à la donnée
Description du association de patient
            LEONA e.V. ist Anlaufstelle für alle seltenen Chromosomenanomalien, ohne eigenes Selbsthilfeangebot. Die Kontaktvermittlung zwischen Betroffenen ist Schwerpunkt. Es werden auch Familien, deren Kinder andere seltene Syndrome, aber vergleichbare Symptome haben oder in der gleichen Region leben vermittelt. Die Selbsthilfe verfügt über 660 Kontaktadressen zu ca. 410 Syndromen. Sie bietet Unterstützung in allen Lebenslagen an: Vom auffälligen Schwangerschaftsbefund und der damit verbundenen Frage, welche Auswirkungen die Störungen haben können, über den Alltag mit chromosomal geschädigten Kindern, Fragen und Problemen zu anstehenden Operationen, Therapien, Therapeuten, Hilfsmitteln bis hin zur Durchsetzung von Ansprüchen gegenüber allen Leistungserbringern. 
Bei aller Seltenheit der einzelnen Diagnosen gibt es auch viele Gemeinsamkeiten: Stärkung und Unterstützung durch das Netzwerk. Dabei hat LEONA kein klassisches Selbsthilfeangebot von regelmäßigen Regionaltreffen. Dazu ist die Anzahl der Betroffenen pro Syndrom zu klein, die Zahl der Diagnosen zu groß. Hilfe findet am Telefon, per E-Mail oder in geschlossenen Internetforen statt. Einmal jährlich findet eine bundesweite Familientagung statt. Das jährlich erscheinende Heft „Einblicke“ mit Berichten der Familien und weiteren Informationen ist nicht nur für die Familien, sondern auch für Fachleute eine wichtige Informationsquelle. Neben den bundesweiten Ansprechpartnern gibt es 31 regionale AnsprechpartnerInnen in Deutschland.
Bei aller Seltenheit der einzelnen Diagnosen gibt es auch viele Gemeinsamkeiten: Stärkung und Unterstützung durch das Netzwerk. Dabei hat LEONA kein klassisches Selbsthilfeangebot von regelmäßigen Regionaltreffen. Dazu ist die Anzahl der Betroffenen pro Syndrom zu klein, die Zahl der Diagnosen zu groß. Hilfe findet am Telefon, per E-Mail oder in geschlossenen Internetforen statt. Einmal jährlich findet eine bundesweite Familientagung statt. Das jährlich erscheinende Heft „Einblicke“ mit Berichten der Familien und weiteren Informationen ist nicht nur für die Familien, sondern auch für Fachleute eine wichtige Informationsquelle. Neben den bundesweiten Ansprechpartnern gibt es 31 regionale AnsprechpartnerInnen in Deutschland.
Care provisions
Cette association de patients offre:
- Forum interne
- Rencontre régulière
- Fédération régionale / Représentant régional
- Newsletter / Magazine de la federation
Aperçu des maladies présentes 1
                    
                        
                        
                        Partial deletion of the short arm of the chromosome X
                        
                    
                        
                        
                        2q24 microdeletion syndrome
                        
                    
                        
                        
                        Tetrasomy 12p
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 20
                        
                    
                        
                        
                        Uniparental disomy of chromosome 14
                        
                    
                        
                        
                        Monosomy 18q
                        
                    
                        
                        
                        X chromosome number anomaly
                        
                    
                        
                        
                        Alagille syndrome due to 20p12 microdeletion
                        
                    
                        
                        
                        Tetraploidy
                        
                    
                        
                        
                        Isochromosome Y
                        
                    
                        
                        
                        Partial duplication of the short arm of chromosome 10
                        
                    
                        
                        
                        Anomaly of chromosome 13
                        
                    
                        
                        
                        Isochromosomy Yp
                        
                    
                        
                        
                        Ring chromosome 4 syndrome
                        
                    
                        
                        
                        Partial duplication/triplication of the short arm of chromosome 5
                        
                    
                        
                        
                        Trisomy 1q
                        
                    
                        
                        
                        Distal duplication 2p
                        
                    
                        
                        
                        Partial duplication of chromosome 2
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 12
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 6
                        
                    
                        
                        
                        Mosaic trisomy 14
                        
                    
                        
                        
                        7q11.23 microduplication syndrome
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 16
                        
                    
                        
                        
                        Ring chromosome 3 syndrome
                        
                    
                        
                        
                        6p22 microdeletion syndrome
                        
                    
                        
                        
                        Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion
                        
                    
                        
                        
                        Inverted duplicated chromosome 15 syndrome
                        
                    
                        
                        
                        15q11q13 microduplication syndrome
                        
                    
                        
                        
                        Partial duplication of the short arm of chromosome 3
                        
                    
                        
                        
                        Paris-Trousseau thrombocytopenia
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 18
                        
                    
                        
                        
                        Partial deletion of chromosome 5
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 14
                        
                    
                        
                        
                        Rubinstein-Taybi syndrome
                        
                    
                        
                        
                        Mosaic trisomy 22
                        
                    
                        
                        
                        Y chromosomal anomaly
                        
                    
                        
                        
                        45,X/46,XY mixed gonadal dysgenesis
                        
                    
                        
                        
                        Ring chromosome 6 syndrome
                        
                    
                        
                        
                        Partial duplication of the short arm of chromosome 8
                        
                    
                        
                        
                        Anomaly of chromosome 8
                        
                    
                        
                        
                        Trisomy 4p
                        
                    
                        
                        
                        Distal duplication 11q
                        
                    
                        
                        
                        Distal duplication 1p36
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 4
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome 22
                        
                    
                        
                        
                        Trisomy X
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 16
                        
                    
                        
                        
                        Distal monosomy 7q36
                        
                    
                        
                        
                        Distal 17p13.3 microdeletion syndrome
                        
                    
                        
                        
                        SATB2-associated syndrome due to a chromosomal rearrangement
                        
                    
                        
                        
                        Partial duplication of chromosome 16
                        
                    
                        
                        
                        17q21.31 microduplication syndrome
                        
                    
                        
                        
                        Ring chromosome 2 syndrome
                        
                    
                        
                        
                        Partial duplication of chromosome 8
                        
                    
                        
                        
                        1q21.1 microduplication syndrome
                        
                    
                        
                        
                        Anomaly of chromosome 2
                        
                    
                        
                        
                        Tetrasomy 18p
                        
                    
                        
                        
                        Paternal uniparental disomy of chromosome 6
                        
                    
                        
                        
                        Partial duplication of the short arm of chromosome 6
                        
                    
                        
                        
                        Uniparental disomy of chromosome 21
                        
                    
                        
                        
                        Turner syndrome due to structural X chromosome anomalies
                        
                    
                        
                        
                        Y chromosome number anomaly
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 2
                        
                    
                        
                        
                        Ring chromosome 7 syndrome
                        
                    
                        
                        
                        Anomaly of chromosome 18
                        
                    
                        
                        
                        2p21 microdeletion syndrome without cystinuria
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 11
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 12
                        
                    
                        
                        
                        Distal duplication 14q
                        
                    
                        
                        
                        Monosomy 9q22.3
                        
                    
                        
                        
                        Partial duplication/triplication of chromosome 5
                        
                    
                        
                        
                        Ring chromosome Y syndrome
                        
                    
                        
                        
                        4p16.3 microduplication syndrome
                        
                    
                        
                        
                        20q11.2 microduplication syndrome
                        
                    
                        
                        
                        Monosomy X
                        
                    
                        
                        
                        14q11.2 microdeletion syndrome
                        
                    
                        
                        
                        Tetrasomy 21
                        
                    
                        
                        
                        Partial deletion of chromosome 18
                        
                    
                        
                        
                        Distal deletion 3p
                        
                    
                        
                        
                        Monosomy 22
                        
                    
                        
                        
                        Trisomy 17p
                        
                    
                        
                        
                        X chromosome anomaly
                        
                    
                        
                        
                        Williams syndrome
                        
                    
                        
                        
                        Triploidy
                        
                    
                        
                        
                        Distal duplication 16q
                        
                    
                        
                        
                        Uniparental disomy of chromosome 7
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 10
                        
                    
                        
                        
                        1q44 microdeletion syndrome
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 20
                        
                    
                        
                        
                        7q31 microdeletion syndrome
                        
                    
                        
                        
                        Distal 16p11.2 microdeletion syndrome
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 9
                        
                    
                        
                        
                        Anomaly of chromosome 12
                        
                    
                        
                        
                        Smith-Magenis syndrome
                        
                    
                        
                        
                        15q13.3 microdeletion syndrome
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome 1
                        
                    
                        
                        
                        2q23.1 microdeletion syndrome
                        
                    
                        
                        
                        Distal 7q11.23 microdeletion syndrome
                        
                    
                        
                        
                        Distal 7q11.23 microduplication syndrome
                        
                    
                        
                        
                        Ring chromosome 8 syndrome
                        
                    
                        
                        
                        Partial deletion of chromosome 8
                        
                    
                        
                        
                        Mosaic trisomy 2
                        
                    
                        
                        
                        Isochromosomy Yq
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 8
                        
                    
                        
                        
                        12q15q21.1 microdeletion syndrome
                        
                    
                        
                        
                        Mosaic trisomy 15
                        
                    
                        
                        
                        16p11.2p12.2 microduplication syndrome
                        
                    
                        
                        
                        Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
                        
                    
                        
                        
                        Distal duplication 13q
                        
                    
                        
                        
                        Distal duplication 3p
                        
                    
                        
                        
                        Monosomy 13q14
                        
                    
                        
                        
                        21q22.11q22.12 microdeletion syndrome
                        
                    
                        
                        
                        3q13 microdeletion syndrome
                        
                    
                        
                        
                        Ring chromosome 5 syndrome
                        
                    
                        
                        
                        Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11
                        
                    
                        
                        
                        Partial duplication of chromosome 19
                        
                    
                        
                        
                        8q21.11 microdeletion syndrome
                        
                    
                        
                        
                        Paternal uniparental disomy of chromosome 5
                        
                    
                        
                        
                        Partial duplication of chromosome 11
                        
                    
                        
                        
                        11p15.4 microduplication syndrome
                        
                    
                        
                        
                        17q12 microduplication syndrome
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 18
                        
                    
                        
                        
                        Tetrasomy 5p
                        
                    
                        
                        
                        Ring chromosome 9 syndrome
                        
                    
                        
                        
                        14q11.2 microduplication syndrome
                        
                    
                        
                        
                        Ring chromosome 13 syndrome
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 17
                        
                    
                        
                        
                        Rare chromosomal anomaly
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 7
                        
                    
                        
                        
                        49,XYYYY syndrome
                        
                    
                        
                        
                        Microtriplication 11q24.1
                        
                    
                        
                        
                        Partial duplication of chromosome 3
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome X
                        
                    
                        
                        
                        Okihiro syndrome due to 20q13 microdeletion
                        
                    
                        
                        
                        Distal 17p13.1 microdeletion syndrome
                        
                    
                        
                        
                        Distal duplication 15q
                        
                    
                        
                        
                        Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
                        
                    
                        
                        
                        Uniparental disomy of chromosome 1
                        
                    
                        
                        
                        Mosaic trisomy 20
                        
                    
                        
                        
                        Silver-Russell syndrome due to 7p11.2p13 microduplication
                        
                    
                        
                        
                        Distal deletion 1q
                        
                    
                        
                        
                        Anomaly of chromosome 20
                        
                    
                        
                        
                        1q41q42 microdeletion syndrome
                        
                    
                        
                        
                        Trisomy 13
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 6
                        
                    
                        
                        
                        Anomaly of chromosome 4
                        
                    
                        
                        
                        Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion
                        
                    
                        
                        
                        Tetrasomy 9p
                        
                    
                        
                        
                        Atypical Norrie disease due to Xp11.3 microdeletion
                        
                    
                        
                        
                        Mosaic monosomy X
                        
                    
                        
                        
                        Distal duplication 7p
                        
                    
                        
                        
                        Miller-Dieker syndrome
                        
                    
                        
                        
                        Distal deletion 6p
                        
                    
                        
                        
                        Sotos syndrome
                        
                    
                        
                        
                        Partial deletion of chromosome 6
                        
                    
                        
                        
                        Paternal uniparental disomy of chromosome 7
                        
                    
                        
                        
                        Partial duplication/triplication of chromosome 9
                        
                    
                        
                        
                        48,XYYY syndrome
                        
                    
                        
                        
                        Ring chromosome 11 syndrome
                        
                    
                        
                        
                        Distal Xq28 microduplication syndrome
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 5
                        
                    
                        
                        
                        16p11.2p12.2 microdeletion syndrome
                        
                    
                        
                        
                        8q22.1 microdeletion syndrome
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 15
                        
                    
                        
                        
                        Partial duplication of chromosome X
                        
                    
                        
                        
                        Trisomy 5p
                        
                    
                        
                        
                        Trisomy 8p
                        
                    
                        
                        
                        Partial deletion of chromosome 12
                        
                    
                        
                        
                        Distal 22q11.2 microdeletion syndrome
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 4
                        
                    
                        
                        
                        X chromosome number anomaly with female phenotype
                        
                    
                        
                        
                        Oculootodental syndrome
                        
                    
                        
                        
                        Mosaic trisomy 16
                        
                    
                        
                        
                        Partial duplication of chromosome 17
                        
                    
                        
                        
                        17q23.1q23.2 microdeletion syndrome
                        
                    
                        
                        
                        Distal duplication 17q
                        
                    
                        
                        
                        10q22.3q23.3 microdeletion syndrome
                        
                    
                        
                        
                        Anomaly of chromosome 14
                        
                    
                        
                        
                        8p11.2 deletion syndrome
                        
                    
                        
                        
                        Proximal 16p11.2 microduplication syndrome
                        
                    
                        
                        
                        15q overgrowth syndrome
                        
                    
                        
                        
                        1p36 deletion syndrome
                        
                    
                        
                        
                        Distal duplication 20q
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 3
                        
                    
                        
                        
                        17q21.31 microdeletion syndrome
                        
                    
                        
                        
                        49,XXXYY syndrome
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 13
                        
                    
                        
                        
                        X-linked intellectual disability-retinitis pigmentosa syndrome
                        
                    
                        
                        
                        Xq27.3q28 duplication syndrome
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 22
                        
                    
                        
                        
                        Partial deletion of chromosome 19
                        
                    
                        
                        
                        Ring chromosome 16 syndrome
                        
                    
                        
                        
                        Deafness-infertility syndrome
                        
                    
                        
                        
                        Anomaly of chromosome 9
                        
                    
                        
                        
                        Paternal uniparental disomy of chromosome 21
                        
                    
                        
                        
                        Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion
                        
                    
                        
                        
                        48,XXXY syndrome
                        
                    
                        
                        
                        Uniparental disomy of chromosome 11
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome 13
                        
                    
                        
                        
                        20p12.3 microdeletion syndrome
                        
                    
                        
                        
                        Mosaic trisomy 1
                        
                    
                        
                        
                        Partial deletion of chromosome 9
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 20
                        
                    
                        
                        
                        Trisomy 18
                        
                    
                        
                        
                        49,XXXXY syndrome
                        
                    
                        
                        
                        Mosaic trisomy 9
                        
                    
                        
                        
                        22q11.2 deletion syndrome
                        
                    
                        
                        
                        2q31.1 microdeletion syndrome
                        
                    
                        
                        
                        Microduplication Xp11.22p11.23 syndrome
                        
                    
                        
                        
                        Partial duplication/triplication of the short arm of chromosome 18
                        
                    
                        
                        
                        Distal deletion 13q
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 10
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 1
                        
                    
                        
                        
                        Mosaic trisomy 4
                        
                    
                        
                        
                        Ring chromosome 1 syndrome
                        
                    
                        
                        
                        Non-distal deletion 12q
                        
                    
                        
                        
                        Partial duplication of chromosome 20
                        
                    
                        
                        
                        12q14 microdeletion syndrome
                        
                    
                        
                        
                        Partial duplication/triplication of the short arm of chromosome 12
                        
                    
                        
                        
                        Distal deletion 7p
                        
                    
                        
                        
                        Partial duplication of the short arm of chromosome 1
                        
                    
                        
                        
                        Potocki-Shaffer syndrome
                        
                    
                        
                        
                        Paternal uniparental disomy of chromosome 20
                        
                    
                        
                        
                        3q29 microdeletion syndrome
                        
                    
                        
                        
                        16p13.11 microduplication syndrome
                        
                    
                        
                        
                        22q11.2 duplication syndrome
                        
                    
                        
                        
                        Ring chromosome 15 syndrome
                        
                    
                        
                        
                        Syndactyly-nystagmus syndrome due to 2q31.1 microduplication
                        
                    
                        
                        
                        Partial duplication of the short arm of chromosome 16
                        
                    
                        
                        
                        Anomaly of chromosome 3
                        
                    
                        
                        
                        Distal deletion 9p
                        
                    
                        
                        
                        X and Y chromosomal anomaly
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 2
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome X
                        
                    
                        
                        
                        20q13.33 microdeletion syndrome
                        
                    
                        
                        
                        Distal triplication 15q
                        
                    
                        
                        
                        Temple syndrome due to paternal 14q32.2 microdeletion
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 18
                        
                    
                        
                        
                        Anomaly of chromosome 19
                        
                    
                        
                        
                        Partial deletion of chromosome 2
                        
                    
                        
                        
                        Sex-chromosome anomaly
                        
                    
                        
                        
                        Distal duplication 22q
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 8
                        
                    
                        
                        
                        8p inverted duplication/deletion syndrome
                        
                    
                        
                        
                        9q31.1q31.3 microdeletion syndrome
                        
                    
                        
                        
                        Proximal Xq28 duplication syndrome
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 7
                        
                    
                        
                        
                        3q26 microduplication syndrome
                        
                    
                        
                        
                        Chromosome Y structural anomaly
                        
                    
                        
                        
                        Mosaic trisomy 8
                        
                    
                        
                        
                        Ring chromosome 10 syndrome
                        
                    
                        
                        
                        16p13.3 microduplication syndrome
                        
                    
                        
                        
                        Distal deletion 19p
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 17
                        
                    
                        
                        
                        14q22q23 microdeletion syndrome
                        
                    
                        
                        
                        Mosaic trisomy 17
                        
                    
                        
                        
                        Partial deletion of chromosome 7
                        
                    
                        
                        
                        Distal duplication 6p
                        
                    
                        
                        
                        Non-distal duplication 9q
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome 4
                        
                    
                        
                        
                        3q27.3 microdeletion syndrome
                        
                    
                        
                        
                        3q29 microduplication syndrome
                        
                    
                        
                        
                        Jacobsen syndrome
                        
                    
                        
                        
                        Paternal uniparental disomy of chromosome 1
                        
                    
                        
                        
                        Xp22.3 microdeletion syndrome
                        
                    
                        
                        
                        7p22.1 microduplication syndrome
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome X
                        
                    
                        
                        
                        WAGR syndrome
                        
                    
                        
                        
                        Partial duplication of the short arm of chromosome 4
                        
                    
                        
                        
                        Trisomy 20p
                        
                    
                        
                        
                        Tetragametic chimerism
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 19
                        
                    
                        
                        
                        Partial duplication/triplication of chromosome 18
                        
                    
                        
                        
                        Partial duplication of chromosome 10
                        
                    
                        
                        
                        16q24.3 microdeletion syndrome
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 15
                        
                    
                        
                        
                        Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14
                        
                    
                        
                        
                        Ring chromosome 12 syndrome
                        
                    
                        
                        
                        Partial duplication/triplication of the short arm of chromosome 9
                        
                    
                        
                        
                        Mesomelia-synostoses syndrome
                        
                    
                        
                        
                        Distal duplication 2q
                        
                    
                        
                        
                        8p23.1 microdeletion syndrome
                        
                    
                        
                        
                        Partial deletion of chromosome 20
                        
                    
                        
                        
                        Non-distal duplication 10q
                        
                    
                        
                        
                        15q24 microdeletion syndrome
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 5
                        
                    
                        
                        
                        Distal deletion 4q
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 17
                        
                    
                        
                        
                        Wolf-Hirschhorn syndrome
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome 2
                        
                    
                        
                        
                        Cat-eye syndrome
                        
                    
                        
                        
                        Deletion 5q35
                        
                    
                        
                        
                        Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
                        
                    
                        
                        
                        6q16 microdeletion syndrome
                        
                    
                        
                        
                        Anomaly of chromosome 5
                        
                    
                        
                        
                        Partial duplication of the short arm of chromosome 7
                        
                    
                        
                        
                        Trichorhinophalangeal syndrome type 2
                        
                    
                        
                        
                        6q terminal deletion syndrome
                        
                    
                        
                        
                        Partial duplication of the short arm of chromosome 2
                        
                    
                        
                        
                        Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
                        
                    
                        
                        
                        3q26q27 microdeletion syndrome
                        
                    
                        
                        
                        Anomaly of chromosome 21
                        
                    
                        
                        
                        Mosaic trisomy 5
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 13
                        
                    
                        
                        
                        47,XYY syndrome
                        
                    
                        
                        
                        Ring chromosome 14 syndrome
                        
                    
                        
                        
                        Proximal 16p11.2 microdeletion syndrome
                        
                    
                        
                        
                        17p11.2 microduplication syndrome
                        
                    
                        
                        
                        20p13 microdeletion syndrome
                        
                    
                        
                        
                        Mosaic trisomy 7
                        
                    
                        
                        
                        Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
                        
                    
                        
                        
                        Distal duplication 5q
                        
                    
                        
                        
                        Mosaic trisomy 10
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 3
                        
                    
                        
                        
                        Partial deletion of chromosome 10
                        
                    
                        
                        
                        Monosomy 9p
                        
                    
                        
                        
                        Monosomy 5p
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 22
                        
                    
                        
                        
                        Distal deletion 10q
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 11
                        
                    
                        
                        
                        2q32q33 microdeletion syndrome
                        
                    
                        
                        
                        X chromosome number anomaly with male phenotype
                        
                    
                        
                        
                        17q12 microdeletion syndrome
                        
                    
                        
                        
                        Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome 9
                        
                    
                        
                        
                        19p13.13 microdeletion syndrome
                        
                    
                        
                        
                        Ring chromosome 17 syndrome
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 1
                        
                    
                        
                        
                        Tetrasomy X
                        
                    
                        
                        
                        Partial deletion of chromosome 3
                        
                    
                        
                        
                        Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 10
                        
                    
                        
                        
                        Anomaly of chromosome 15
                        
                    
                        
                        
                        Chromosome X structural anomaly
                        
                    
                        
                        
                        Mowat-Wilson syndrome due to monosomy 2q22
                        
                    
                        
                        
                        Partial chromosome Y deletion
                        
                    
                        
                        
                        Distal duplication 4q
                        
                    
                        
                        
                        Non-distal monosomy 20q
                        
                    
                        
                        
                        Uniparental disomy of chromosome 15
                        
                    
                        
                        
                        Trisomy 10p
                        
                    
                        
                        
                        Kleefstra syndrome due to 9q34 microdeletion
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 19
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome 6
                        
                    
                        
                        
                        Partial duplication of chromosome 6
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 9
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 8
                        
                    
                        
                        
                        Anomaly of chromosome 10
                        
                    
                        
                        
                        2p15p16.1 microdeletion syndrome
                        
                    
                        
                        
                        19q13.11 microdeletion syndrome
                        
                    
                        
                        
                        Partial deletion of chromosome 16
                        
                    
                        
                        
                        FOXG1 syndrome due to 14q12 microdeletion
                        
                    
                        
                        
                        12p12.1 microdeletion syndrome
                        
                    
                        
                        
                        Ring chromosome 18 syndrome
                        
                    
                        
                        
                        Trisomy 18p
                        
                    
                        
                        
                        48,XXYY syndrome
                        
                    
                        
                        
                        Polyploidy
                        
                    
                        
                        
                        Prader-Willi syndrome due to paternal 15q11q13 deletion
                        
                    
                        
                        
                        Mosaic trisomy 12
                        
                    
                        
                        
                        Anomaly of chromosome 7
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 7
                        
                    
                        
                        
                        Xp21 deletion syndrome
                        
                    
                        
                        
                        Distal deletion 15q
                        
                    
                        
                        
                        Distal deletion 14q
                        
                    
                        
                        
                        Partial deletion of chromosome 1
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 16
                        
                    
                        
                        
                        Monosomy 13q34
                        
                    
                        
                        
                        Ring chromosome 19 syndrome
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 6
                        
                    
                        
                        
                        4q21 microdeletion syndrome
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome 16
                        
                    
                        
                        
                        DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
                        
                    
                        
                        
                        8p23.1 duplication syndrome
                        
                    
                        
                        
                        Uniparental disomy of chromosome 13
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 5
                        
                    
                        
                        
                        5q14.3 microdeletion syndrome
                        
                    
                        
                        
                        Pentasomy X
                        
                    
                        
                        
                        14q24.1q24.3 microdeletion syndrome
                        
                    
                        
                        
                        17q11 microdeletion syndrome
                        
                    
                        
                        
                        Distal deletion 12p
                        
                    
                        
                        
                        Trisomy 12p
                        
                    
                        
                        
                        Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
                        
                    
                        
                        
                        Distal duplication 18q
                        
                    
                        
                        
                        Partial deletion of chromosome X
                        
                    
                        
                        
                        Anomaly of chromosome 17
                        
                    
                        
                        
                        Autosomal anomaly
                        
                    
                        
                        
                        21q deletion syndrome
                        
                    
                        
                        
                        1p31p32 microdeletion syndrome
                        
                    
                        
                        
                        Familial clubfoot due to 17q23.1q23.2 microduplication
                        
                    
                        
                        
                        Distal deletion 17q
                        
                    
                        
                        
                        5p13 microduplication syndrome
                        
                    
                        
                        
                        Anomaly of chromosome 1
                        
                    
                        
                        
                        Turner syndrome
                        
                    
                        
                        
                        Partial duplication of chromosome 1
                        
                    
                        
                        
                        Distal deletion 10p
                        
                    
                        
                        
                        Distal duplication 6q
                        
                    
                        
                        
                        Partial deletion of chromosome 11
                        
                    
                        
                        
                        Distal deletion 12q
                        
                    
                        
                        
                        Temple syndrome due to maternal uniparental disomy of chromosome 14
                        
                    
                        
                        
                        1p21.3 microdeletion syndrome
                        
                    
                        
                        
                        16q24.1 microdeletion syndrome
                        
                    
                        
                        
                        16p13.11 microdeletion syndrome
                        
                    
                        
                        
                        17q11.2 microduplication syndrome
                        
                    
                        
                        
                        Recombinant 8 syndrome
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 14
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 4
                        
                    
                        
                        
                        X small rings
                        
                    
                        
                        
                        Rubinstein-Taybi syndrome due to CREBBP mutations
                        
                    
                        
                        
                        Ring chromosome 20 syndrome
                        
                    
                        
                        
                        Mosaic trisomy 3
                        
                    
                        
                        
                        Xq12-q13.3 duplication syndrome
                        
                    
                        
                        
                        Distal duplication 19q
                        
                    
                        
                        
                        Otodental syndrome
                        
                    
                        
                        
                        X-linked Alport syndrome-diffuse leiomyomatosis
                        
                    
                        
                        
                        Mosaic variegated aneuploidy syndrome
                        
                    
                        
                        
                        Uniparental disomy of chromosome X
                        
                    
                        
                        
                        Paternal 20q13.2q13.3 microdeletion syndrome
                        
                    
                        
                        
                        2q37 microdeletion syndrome
                        
                    
                        
                        
                        Monosomy 22q13.3
                        
                    
                        
                        
                        10q22.3q23.3 microduplication syndrome
                        
                    
                        
                        
                        9p13 microdeletion syndrome
                        
                    
                        
                        
                        Partial deletion of chromosome 4
                        
                    
                        
                        
                        17p13.3 microduplication syndrome
                        
                    
                        
                        
                        Non-distal deletion 10q
                        
                    
                        
                        
                        Anomaly of chromosome 11
                        
                    
                        
                        
                        Angelman syndrome due to paternal uniparental disomy of chromosome 15
                        
                    
                        
                        
                        Monosomy 18p
                        
                    
                        
                        
                        Partial duplication of the long arm of chromosome 11
                        
                    
                        
                        
                        Partial deletion of the short arm of chromosome 2
                        
                    
                        
                        
                        Distal duplication 9q
                        
                    
                        
                        
                        1q21.1 microdeletion syndrome
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 21
                        
                    
                        
                        
                        Ring chromosome 21 syndrome
                        
                    
                        
                        
                        Homozygous 2p21 microdeletion syndrome
                        
                    
                        
                        
                        Distal duplication 10q
                        
                    
                        
                        
                        Trisomy 8q
                        
                    
                        
                        
                        Emanuel syndrome
                        
                    
                        
                        
                        Partial duplication of chromosome 7
                        
                    
                        
                        
                        Non-distal monosomy 7p
                        
                    
                        
                        
                        Paternal uniparental disomy of chromosome 13
                        
                    
                        
                        
                        Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
                        
                    
                        
                        
                        8q12 microduplication syndrome
                        
                    
                        
                        
                        Maternal uniparental disomy of chromosome 21
                        
                    
                        
                        
                        Anomaly of chromosome 6
                        
                    
                        
                        
                        Xp22.13p22.2 duplication syndrome
                        
                    
                        
                        
                        Uniparental disomy of chromosome 20
                        
                    
                        
                        
                        Partial deletion of the long arm of chromosome 3
                        
                    
                        
                        
                        Syndrome de microdélétion 2p13.2
                        
                    
                        
                        
                        Syndrome de microduplication 22q11.2 distale
                        
                    
                        
                        
                        Syndrome de Silver-Russell dû à une microduplication 11p15
                        
                    
                        
                        
                        Syndrome de microduplication 2q23.1
                        
                    
                        
                        
                        Duplication partielle du bras court du chromosome X
                        
                    
                        
                        
                        Syndrome de microdélétion 6q25
                        
                    
                        
                        
                        Délétion partielle du bras long du chromosome 19
                        
                    
                        
                        
                        Anomalie du chromosome 22
                        
                    
                        
                        
                        Syndrome d'Angelman dû à une délétion 15q11q13 d'origine maternelle
                        
                    
                        
                        
                        Duplication partielle du bras court du chromosome 17
                        
                    
                        
                        
                        Syndrome de dysmorphie craniofaciale-anomalies squelettiques-cardiopathie-trouble neurologique du développement dû à une microdélétion 9q21.3
                        
                    
                        
                        
                        Syndrome de microdélétion 15q11.2
                        
                    
                        
                        
                        Duplication partielle du chromosome 4
                        
                    
                        
                        
                        Duplication partielle du bras long du chromosome 9
                        
                    
                        
                        
                        Disomie uniparentale paternelle du chromosome X
                        
                    
                        
                        
                        Délétion partielle du chromosome 17
                        
                    
                        
                        
                        Duplication distale 8q
                        
                    
                        
                        
                        Délétion partielle du bras long du chromosome 1
                        
                    
                        
                        
                        Disomie uniparentale du chromosome 6
                        
                    
                        
                        
                        Polysomie du chromosome X
                        
                    
                        
                        
                        Monosomie distale 20q
                        
                    
                        
                        
                        Syndrome du chromosome 22 en anneau
                        
                    
                        
                        
                        Disomie uniparentale maternelle du chromosome 20
                        
                    
                        
                        
                        Duplication partielle du bras court du chromosome 11
                        
                    
                        
                        
                        Anomalie du chromosome 16
                        
                    
                        
                        
                        Syndrome de microduplication 5q35
                        
                    
                        
                        
                        Duplication non distale 13q
                        
                    
                        
                        
                        Syndrome de microdélétion 19p13.12
                        
                    
                        
                        
                        Trisomie 9p
                        
                    
                
            7.62869751563122251.485776400000006LEONA e.V. - Familienselbsthilfe bei seltenen chromosomalen Veränderungen
            
        Dernière modification:
        25.10.2023
    
