SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Zentrum für seltene Entwicklungsstörungen am kbo-Kinderzentrum München

Description of facility

Director / Spokesperson
Dr. med. Marta Somorai
Information
Care facility for children
Description
Zwischen Entwicklungsstörungen und seltenen Erkrankungen besteht ein enger Zusammenhang. Störungen der Entwicklung sind eine häufige Manifestation seltener Erkrankungen einerseits, die häufigste Ursache von Entwicklungsstörungen andererseits sind seltene Erkrankungen. Das kbo-Kinderzentrum ist ein Zentrum mit weit überregionalem Einzugsgebiet für Fragestellung rund um die Diagnostik und Therapie von Entwicklungsstörungen. Im Mittelpunkt steht die interdisziplinäre und ganzheitliche Betreuung der Patienten unter Einbeziehung der Eltern. So hält das Zentrum eines der umfassendsten Angebote an Eltern- und Patientenschulungen bundesweit vor. Besondere diagnostische Schwerpunkte sind die Genetik, die Psychologische Diagnostik und die Pädaudiologie. Therapeutische Schwerpunkte sind die psychologische Therapie und Interaktionstherapie, die Physio-, Ergo-, Logo- und Musiktherapie, sowie die Pharmakotherapie.

Consultation hours

nach Vereinbarung.

Care provisions

This facility offers the following
  • Social / legal advice
  • Genetic counselling
  • Clinical studies / research
  • Diagnostic
  • Therapy
  • Contact person for patients with an unclear diagnosis

Contact

Dr. med. Marta Somorai
089 710090
089 71009253
ZSEamKIZ@kbo.de
Website http://www.kbo-kinderzentrum-muenchen.de

Secondary Contact

089 71009318

Address

Heiglhofstr. 65
81377 München

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch
France.png Französisch
Turkey.png Türkisch

Preview of the assigned diseases 12

Dysmorphism-short stature-deafness-difference of sex development syndrome S-adenosylhomocysteine hydrolase deficiency Coffin-Siris syndrome Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome COFS syndrome Hypotonia-speech impairment-severe cognitive delay syndrome Nodular neuronal heterotopia Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome Syndromic multisystem autoimmune disease due to Itch deficiency Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome Solitary median maxillary central incisor syndrome Mowat-Wilson syndrome 3-phosphoserine phosphatase deficiency, infantile/juvenile form Short ulna-dysmorphism-hypotonia-intellectual disability syndrome Polymicrogyria due to TUBB2B mutation PYCR2-related microcephaly-progressive leukoencephalopathy 9q31.1q31.3 microdeletion syndrome 3q27.3 microdeletion syndrome Intellectual disability-epilepsy-extrapyramidal syndrome Aniridia-renal agenesis-psychomotor retardation syndrome Bannayan-Riley-Ruvalcaba syndrome Aniridia-cerebellar ataxia-intellectual disability syndrome Macrocephaly-spastic paraplegia-dysmorphism syndrome X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome Hirsutism-skeletal dysplasia-intellectual disability syndrome Cardiofaciocutaneous syndrome Aniridia-ptosis-intellectual disability-familial obesity syndrome Semilobar holoprosencephaly Aniridia-intellectual disability syndrome Holoprosencephaly 2q23.1 microduplication syndrome Hyperphosphatasia-intellectual disability syndrome Global developmental delay-osteopenia-ectodermal defect syndrome Filippi syndrome Autosomal recessive spastic paraplegia type 9B Moynahan syndrome Czeizel-Losonci syndrome Holoprosencephaly-postaxial polydactyly syndrome Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome Alopecia-intellectual disability syndrome Intellectual disability-facial dysmorphism-hand anomalies syndrome Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome Corpus callosum agenesis-macrocephaly-hypertelorism syndrome Ossification anomalies-psychomotor developmental delay syndrome Oculo-palato-cerebral syndrome Pterygium colli-intellectual disability-digital anomalies syndrome Shoulder and girdle defects-familial intellectual disability syndrome X-linked syndromic intellectual disability Syndromic neurometabolic disease with non-X-linked intellectual disability Microcephaly-glomerulonephritis-marfanoid habitus syndrome Congenital heart defect-round face-developmental delay syndrome 3-methylglutaconic aciduria type 7 PGM3-CDG Spondyloepiphyseal dysplasia tarda, Kohn type Ulbright-Hodes syndrome Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome Say-Barber-Miller syndrome Johanson-Blizzard syndrome 16p12.1p12.3 triplication syndrome Blepharophimosis-intellectual disability syndrome MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect Floating-Harbor syndrome 3p25.3 microdeletion syndrome Hereditary cryohydrocytosis with reduced stomatin Urban-Rogers-Meyer syndrome Short stature-webbed neck-heart disease syndrome Spondylocostal dysostosis-hypospadias-intellectual disability syndrome Intellectual disability-brachydactyly-Pierre Robin syndrome Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome 13q12.3 microdeletion syndrome Kabuki syndrome Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome Facial dysmorphism-shawl scrotum-joint laxity syndrome Sanjad-Sakati syndrome Congenital non-communicating hydrocephalus Osteopenia-intellectual disability-sparse hair syndrome 3C syndrome Wolf-Hirschhorn syndrome Marfanoid habitus-autosomal recessive intellectual disability syndrome Polymicrogyria with optic nerve hypoplasia Kagami-Ogata syndrome Kapur-Toriello syndrome Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome ANE syndrome Cataract-hypertrichosis-intellectual disability syndrome Crane-Heise syndrome KBG syndrome 5p13 microduplication syndrome Fryns syndrome Spastic paraplegia-severe developmental delay-epilepsy syndrome Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome Temple syndrome due to paternal 14q32.2 microdeletion Achondroplasia Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome Cataract-nephropathy-encephalopathy syndrome Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency Cataract-intellectual disability-anal atresia-urinary defects syndrome Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome Galloway-Mowat syndrome Combined oxidative phosphorylation defect type 7 Septo-optic dysplasia spectrum AICA-ribosiduria Zechi-Ceide syndrome Primary non-essential cutis verticis gyrata DYRK1A-related intellectual disability syndrome Microcephaly-brachydactyly-kyphoscoliosis syndrome Cataract-intellectual disability-hypogonadism syndrome Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome Megalocornea-intellectual disability syndrome MMEP syndrome Catel-Manzke syndrome Cortical blindness-intellectual disability-polydactyly syndrome Blepharonasofacial malformation syndrome Xeroderma pigmentosum-Cockayne syndrome complex Microcephalic primordial dwarfism, Montreal type RARS-related autosomal recessive hypomyelinating leukodystrophy Temple syndrome due to maternal uniparental disomy of chromosome 14 Omphalocele syndrome, Shprintzen-Goldberg type Orofaciodigital syndrome type 10 Temple syndrome due to paternal 14q32.2 hypomethylation Angelman syndrome due to imprinting defect in 15q11-q13 Wiedemann-Steiner syndrome Hypertelorism-microtia-facial clefting syndrome Fallot complex-intellectual disability-growth delay syndrome 17q11 microdeletion syndrome Cockayne syndrome type 3 Caudal appendage-deafness syndrome White-Sutton syndrome Cockayne syndrome type 2 Biemond syndrome type 2 Upper limb defect-eye and ear abnormalities syndrome 9q33.3q34.11 microdeletion syndrome Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome Acrocallosal syndrome Agnathia-holoprosencephaly-situs inversus syndrome Rare genetic intellectual disability Prominent glabella-microcephaly-hypogenitalism syndrome Arachnodactyly-abnormal ossification-intellectual disability syndrome Polyendocrine-polyneuropathy syndrome Weaver-Williams syndrome Macrocephaly-developmental delay syndrome Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome Epilepsy-microcephaly-skeletal dysplasia syndrome Intellectual disability-strabismus syndrome Infantile spasms syndrome Bowen-Conradi syndrome Epilepsy-telangiectasia syndrome Orofaciodigital syndrome type 14 Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome Septopreoptic holoprosencephaly Aymé-Gripp syndrome Hair defect-photosensitivity-intellectual disability syndrome Phosphoserine aminotransferase deficiency, infantile/juvenile form Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome 20q11.2 microduplication syndrome Angelman syndrome due to paternal uniparental disomy of chromosome 15 Angelman syndrome due to maternal 15q11q13 deletion Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome Bohring-Opitz syndrome Holoprosencephaly-radial heart renal anomalies syndrome Aicardi-Goutières syndrome Lissencephaly Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome Epiphyseal dysplasia-hearing loss-dysmorphism syndrome 3MC syndrome Down syndrome Basel-Vanagaite-Smirin-Yosef syndrome Proximal 16p11.2 microduplication syndrome Woodhouse-Sakati syndrome Micro syndrome Grubben-de Cock-Borghgraef syndrome Hypomyelination-congenital cataract syndrome Transketolase deficiency Cohen syndrome Laurence-Moon syndrome 2p13.2 microdeletion syndrome GMS syndrome Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome Prolidase deficiency 8q21.11 microdeletion syndrome Hall-Riggs syndrome Cornelia de Lange syndrome Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome Hallermann-Streiff syndrome Middle and/or inner ear anomaly Complex lethal osteochondrodysplasia Zimmermann-Laband syndrome Microcephaly-seizures-intellectual disability-heart disease syndrome Severe intellectual disability and progressive spastic paraplegia Microcephaly-cleft palate-abnormal retinal pigmentation syndrome Cerebrooculonasal syndrome Lenz-Majewski hyperostotic dwarfism Microcephaly-cervical spine fusion anomalies syndrome Severe intellectual disability-progressive spastic diplegia syndrome Sturge-Weber syndrome Intellectual disability-myopathy-short stature-endocrine defect syndrome Harrod syndrome White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome Hartsfield syndrome Costello syndrome Goldberg-Shprintzen megacolon syndrome Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome Branchioskeletogenital syndrome Autosomal dominant non-syndromic intellectual disability Angelman syndrome Intellectual disability-short stature-hypertelorism syndrome CEDNIK syndrome Early-onset epilepsy-intellectual disability-brain anomalies syndrome Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome Rare non-syndromic intellectual disability TBCK-related intellectual disability syndrome Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome Ptosis-syndactyly-learning difficulties syndrome Intellectual disability, Wolff type WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome C syndrome Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome Neurofaciodigitorenal syndrome Fountain syndrome Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome Intellectual disability-polydactyly-uncombable hair syndrome Fatty acyl-CoA reductase 1 deficiency Hypotrichosis-intellectual disability, Lopes type Intellectual disability-hyperkinetic movement-truncal ataxia syndrome Skeletal dysplasia-epilepsy-short stature syndrome 17q11.2 microduplication syndrome Neuroectodermal-endocrine syndrome 2q23.1 microdeletion syndrome Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome Alobar holoprosencephaly Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Lobar holoprosencephaly Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome Hennekam syndrome Neurofibromatosis type 1 Atypical autism Lowry-MacLean syndrome Midline interhemispheric variant of holoprosencephaly Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia Microcephaly-thin corpus callosum-intellectual disability syndrome 15q24 microdeletion syndrome Isolated anencephaly/exencephaly Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome Keutel syndrome Hernández-Aguirre Negrete syndrome PDE4D haploinsufficiency syndrome Genitopatellar syndrome Deafness-onychodystrophy syndrome X-linked non-syndromic intellectual disability Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome Ramos-Arroyo syndrome Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome Dubowitz syndrome Pyridoxal phosphate-responsive seizures Laminin subunit alpha 2-related congenital muscular dystrophy X-linked intellectual disability, Stocco Dos Santos type Treacher-Collins syndrome Pfeiffer-Palm-Teller syndrome 16p13.3 microduplication syndrome Blepharophimosis-intellectual disability syndrome, MKB type Pitt-Hopkins syndrome Intellectual disability-cataracts-kyphosis syndrome Autosomal dominant Charcot-Marie-Tooth disease type 2Z Intellectual disability-spasticity-ectrodactyly syndrome Oliver syndrome 12q14 microdeletion syndrome Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome Angelman syndrome due to a point mutation Partial deletion of the long arm of chromosome 1 Autosomal recessive spastic paraplegia type 55 Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome Williams syndrome Myoclonic-astatic epilepsy Intellectual disability-expressive aphasia-facial dysmorphism syndrome THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome Baraitser-Winter cerebrofrontofacial syndrome Cono-spondylar dysplasia Acrocardiofacial syndrome Tatton-Brown-Rahman syndrome Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome Cleft palate-short stature-vertebral anomalies syndrome DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion Intellectual disability-cataracts-calcified pinnae-myopathy syndrome FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome Blepharophimosis-intellectual disability syndrome, SBBYS type Nicolaides-Baraitser syndrome Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Camptodactyly syndrome, Guadalajara type 3 Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome Rubinstein-Taybi syndrome due to CREBBP mutations 22q11.2 deletion syndrome Koolen-De Vries syndrome Wiedemann-Rautenstrauch syndrome Pierpont syndrome Marden-Walker syndrome Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome McDonough syndrome DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy Witteveen-Kolk syndrome Contractures-ectodermal dysplasia-cleft lip/palate syndrome Microbrachycephaly-ptosis-cleft lip syndrome Mitochondrial oxidative phosphorylation disorder Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Craniodigital-intellectual disability syndrome 19p13.3 microduplication syndrome Cantú syndrome 3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome Monosomy 22q13.3 Intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome Xp22.13p22.2 duplication syndrome Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome Myopathy-growth delay-intellectual disability-hypospadias syndrome Autosomal recessive non-syndromic intellectual disability Pontine autosomal dominant microangiopathy with leukoencephalopathy Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome Monosomy 18p Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome Autosomal dominant Charcot-Marie-Tooth disease type 2O SLC35A2-CDG Neurofibromatosis-Noonan syndrome Noonan syndrome Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome Lethal omphalocele-cleft palate syndrome Isolated congenital auditory ossicle malformation Osteopathia striata-cranial sclerosis syndrome Osteopetrosis with renal tubular acidosis Sinoatrial node dysfunction and deafness Dysequilibrium syndrome SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome Pachygyria-intellectual disability-epilepsy syndrome Distal nebulin myopathy Acrofacial dysostosis, Rodríguez type Spastic paraplegia-glaucoma-intellectual disability syndrome Usher syndrome type 1 Autosomal recessive spastic paraplegia type 11 Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome RERE-related neurodevelopmental syndrome Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome Smith-Lemli-Opitz syndrome Freeman-Sheldon syndrome Orofaciodigital syndrome type 3 Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome Cockayne syndrome Radioulnar synostosis-developmental delay-hypotonia syndrome 8p23.1 duplication syndrome Congenital cataracts-facial dysmorphism-neuropathy syndrome 2-aminoadipic 2-oxoadipic aciduria Lennox-Gastaut syndrome Waardenburg-Shah syndrome CHD3-related developmental delay-speech delay-intellectual disability-abnormalities of vision-facial dysmorphism syndrome CTCF-related neurodevelopmental disorder Familial paroxysmal ataxia Distal 16p11.2 microdeletion syndrome 1q21.1 microduplication syndrome CHARGE syndrome Trisomy 1q Rubinstein-Taybi syndrome due to 16p13.3 microdeletion GAPO syndrome Adenylosuccinate lyase deficiency 1p21.3 microdeletion syndrome 15q11.2 microdeletion syndrome Alström syndrome Proximal 16p11.2 microdeletion syndrome Alternating hemiplegia of childhood Bardet-Biedl syndrome Beckwith-Wiedemann syndrome 16p13.11 microduplication syndrome Stimmler syndrome Distal 17p13.3 microdeletion syndrome Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Microcephalic primordial dwarfism 1q44 microdeletion syndrome FOXP1 Syndrome Cockayne syndrome type 1 Intellectual disability, Birk-Barel type Autism spectrum disorder due to AUTS2 deficiency Primary hyperaldosteronism-seizures-neurological abnormalities syndrome Intellectual disability-seizures-macrocephaly-obesity syndrome X-linked intellectual disability, Cabezas type Bainbridge-Ropers syndrome Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome Microduplication Xp11.22p11.23 syndrome Mowat-Wilson syndrome due to monosomy 2q22 Spastic paraplegia type 7 Usher syndrome type 2 Developmental delay-facial dysmorphism syndrome due to MED13L deficiency Hypospadias-intellectual disability, Goldblatt type syndrome Bonnemann-Meinecke-Reich syndrome Brachydactyly-mesomelia-intellectual disability-heart defects syndrome Mandibulofacial dysostosis-microcephaly syndrome Johnson neuroectodermal syndrome Joubert syndrome with oculorenal defect Monosomy 5p Infantile choroidocerebral calcification syndrome Microphthalmia-brain atrophy syndrome Noonan syndrome with multiple lentigines Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome Gómez-López-Hernández syndrome Partial duplication/triplication of the short arm of chromosome 12 14q24.1q24.3 microdeletion syndrome Cryptorchidism-arachnodactyly-intellectual disability syndrome HANAC syndrome Myhre syndrome Developmental and speech delay due to SOX5 deficiency X-linked intellectual disability-hypotonia-movement disorder syndrome MEND syndrome Temple syndrome Combined oxidative phosphorylation defect type 27 Short stature-advanced bone age-early-onset osteoarthritis syndrome 11q22.2q22.3 microdeletion syndrome Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome Partial duplication of the short arm of chromosome 10 Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome Pyridoxine-dependent epilepsy Qazi-Markouizos syndrome Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome C12ORF65-related combined oxidative phosphorylation defect Pitt-Hopkins-like syndrome Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency Alacrimia-choreoathetosis-liver dysfunction syndrome Intellectual disability-balding-patella luxation-acromicria syndrome Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome Seizures-scoliosis-macrocephaly syndrome Alopecia-contractures-dwarfism-intellectual disability syndrome Hepatic fibrosis-renal cysts-intellectual disability syndrome Atelosteogenesis type II Atelosteogenesis type III VPS11-related autosomal recessive hypomyelinating leukodystrophy Osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Rubinstein-Taybi syndrome ADNP syndrome Cataract-deafness-hypogonadism syndrome Microcephaly-micromelia syndrome Kleefstra syndrome Optic atrophy-intellectual disability syndrome Weaver syndrome Shprintzen-Goldberg syndrome AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome Short stature-brachydactyly-obesity-global developmental delay syndrome Intellectual disability syndrome due to a DYRK1A point mutation Uveal coloboma-cleft lip and palate-intellectual disability Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Spinocerebellar ataxia type 6 Autosomal recessive primary microcephaly Rare genetic syndromic intellectual disability Microcephaly-cardiomyopathy syndrome Non-specific early-onset epileptic encephalopathy Microcephaly-microcornea syndrome, Seemanova type Familial porencephaly Microcephaly-deafness-intellectual disability syndrome Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome 20q11.2 microdeletion syndrome Okamoto syndrome Cerebellar-facial-dental syndrome 17p11.2 microduplication syndrome Microcephaly-polymicrogyria-corpus callosum agenesis syndrome Orofaciodigital syndrome type 6 Intellectual disability-alacrima-achalasia syndrome 9p13 microdeletion syndrome Osteoporosis-pseudoglioma syndrome Temtamy syndrome Acrofacial dysostosis, Catania type Spastic paraplegia-epilepsy-intellectual disability syndrome Partial deletion of the short arm of chromosome 9 Smith-Magenis syndrome Cardiocranial syndrome, Pfeiffer type Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome MEDNIK syndrome Alpha-thalassemia-X-linked intellectual disability syndrome Orofaciodigital syndrome type 5 Preaxial polydactyly-colobomata-intellectual disability syndrome 15q11q13 microduplication syndrome PCNA-related progressive neurodegenerative photosensitivity syndrome Porencephaly Congenital insensitivity to pain with severe intellectual disability Spondylocostal dysostosis-anal atresia-genitourinary malformation syndrome Difference of sex development-intellectual disability syndrome Pseudoprogeria syndrome Severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome Distal monosomy 7q36 Combined oxidative phosphorylation defect type 23 Diastrophic dysplasia Microlissencephaly-micromelia syndrome Brain malformation-congenital heart disease-postaxial polydactyly syndrome PMP22-RAI1 contiguous gene duplication syndrome ANK3-related intellectual disability-sleep disturbance syndrome Megalencephaly-severe kyphoscoliosis-overgrowth syndrome 19p13.13 microdeletion syndrome Oculocerebrofacial syndrome, Kaufman type Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome Orofaciodigital syndrome type 2 Orofaciodigital syndrome type 4 Temple-Baraitser syndrome Distal 17p13.1 microdeletion syndrome SLC39A8-CDG Non-specific syndromic intellectual disability Intellectual disability, Buenos-Aires type Atypical Rett syndrome Crouzon syndrome-acanthosis nigricans syndrome 6q terminal deletion syndrome Sialuria Congenital contractural arachnodactyly X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency Polymicrogyria 7q31 microdeletion syndrome TELO2-related intellectual disability-neurodevelopmental disorder Chudley-McCullough syndrome Inverted duplicated chromosome 15 syndrome KDM5C-related syndromic X-linked intellectual disability Dravet syndrome Juvenile myoclonic epilepsy Malignant migrating focal seizures of infancy Simpson-Golabi-Behmel syndrome Keppen-Lubinsky syndrome Rare autosomal dominant non-syndromic sensorineural deafness type DFNA Infantile bilateral striatal necrosis Bilateral generalized polymicrogyria Menke-Hennekam syndrome GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder Developmental delay with autism spectrum disorder and gait instability Larsen syndrome Rare autosomal recessive non-syndromic sensorineural deafness type DFNB Kleefstra syndrome due to a point mutation Periventricular nodular heterotopia GNB5-related intellectual disability-cardiac arrhythmia syndrome GNAO1-related developmental delay-seizures-movement disorder spectrum Episodic ataxia type 1 Axenfeld-Rieger syndrome Childhood absence epilepsy Autosomal recessive spastic paraplegia type 77 Early infantile epileptic encephalopathy Kleefstra syndrome due to 9q34 microdeletion Isolated childhood apraxia of speech 5q14.3 microdeletion syndrome Allan-Herndon-Dudley syndrome Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion L1 syndrome Congenital communicating hydrocephalus X-linked creatine transporter deficiency Malan overgrowth syndrome Joubert syndrome Autosomal dominant dopa-responsive dystonia Alagille syndrome due to a NOTCH2 point mutation NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance X-linked intellectual disability-cerebellar hypoplasia syndrome Autosomal dominant epilepsy with auditory features Biotin-thiamine-responsive basal ganglia disease Rett syndrome Silver-Russell syndrome 47,XYY syndrome 48,XXYY syndrome SMARCA2-related blepharophimosis-intellectual disability syndrome Barth syndrome SYNGAP1-related developmental and epileptic encephalopathy 2q24 microdeletion syndrome Sotos syndrome STXBP1-related encephalopathy Mowat-Wilson syndrome due to a ZEB2 point mutation X-linked intellectual disability-short stature-overweight syndrome Lamb-Shaffer syndrome Beta-propeller protein-associated neurodegeneration Autosomal dominant spastic paraplegia type 8 Weiss-Kruszka Syndrome
11.47860467433929648.10682940641875Zentrum für seltene Entwicklungsstörungen am kbo-Kinderzentrum München
Last updated: 10.01.2024