Mosaic variegated aneuploidy syndrome
All Entries 4
Zentrum für Seltene Endokrine Erkrankungen (hormonelle Erkrankungen) am Universitätsklinikum Ulm
Universitätsklinikum Ulm Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm
Eythstraße 24
89075 Ulm
0731 50057401
0731 50057407
Page Web
Email
- Rare diabetes mellitus
- Acquired lipodystrophy
- Craniopharyngioma
- Prolactinoma
- Genetic obesity
- Pseudohypoparathyroidism type 1A
- Congenital hypogonadotropic hypogonadism
- Multiple endocrine neoplasia
- Congenital isolated hyperinsulinism
- Central diabetes insipidus
- Addison disease
- Primary lipodystrophy
- Acromegaly
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
Page Web
Email
- Noonan syndrome
- Li-Fraumeni syndrome
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Familial ovarian cancer
- Inherited cancer-predisposing syndrome
- Diamond-Blackfan anemia
- Common variable immunodeficiency
- Ataxia-telangiectasia
- Full NF2-related schwannomatosis
- Silver-Russell syndrome
- Hereditary nonpolyposis colon cancer
- Hereditary retinoblastoma
- Constitutional mismatch repair deficiency syndrome
- Von Hippel-Lindau disease
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Page Web
Email
- Familial ovarian cancer
- Maffucci syndrome
- Costello syndrome
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Ataxia-telangiectasia
- Silver-Russell syndrome
- Cockayne syndrome
- Diamond-Blackfan anemia
- Inherited renal cancer-predisposing syndrome
- Li-Fraumeni syndrome
- Full NF2-related schwannomatosis
- Noonan syndrome
- APC-related attenuated familial adenomatous polyposis
- Von Hippel-Lindau disease
LEONA e.V. - Familienselbsthilfe bei seltenen chromosomalen Veränderungen
Kornblumenweg 38
59439
Holzwickede
Institutions de rang supérieur 0
Conseil génétique 2
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
Page Web
Email
- Noonan syndrome
- Li-Fraumeni syndrome
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Familial ovarian cancer
- Inherited cancer-predisposing syndrome
- Diamond-Blackfan anemia
- Common variable immunodeficiency
- Ataxia-telangiectasia
- Full NF2-related schwannomatosis
- Silver-Russell syndrome
- Hereditary nonpolyposis colon cancer
- Hereditary retinoblastoma
- Constitutional mismatch repair deficiency syndrome
- Von Hippel-Lindau disease
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Page Web
Email
- Familial ovarian cancer
- Maffucci syndrome
- Costello syndrome
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Ataxia-telangiectasia
- Silver-Russell syndrome
- Cockayne syndrome
- Diamond-Blackfan anemia
- Inherited renal cancer-predisposing syndrome
- Li-Fraumeni syndrome
- Full NF2-related schwannomatosis
- Noonan syndrome
- APC-related attenuated familial adenomatous polyposis
- Von Hippel-Lindau disease
Institutions de prise en charge 1
Zentrum für Seltene Endokrine Erkrankungen (hormonelle Erkrankungen) am Universitätsklinikum Ulm
Universitätsklinikum Ulm Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm
Eythstraße 24
89075 Ulm
0731 50057401
0731 50057407
Page Web
Email
- Rare diabetes mellitus
- Acquired lipodystrophy
- Craniopharyngioma
- Prolactinoma
- Genetic obesity
- Pseudohypoparathyroidism type 1A
- Congenital hypogonadotropic hypogonadism
- Multiple endocrine neoplasia
- Congenital isolated hyperinsulinism
- Central diabetes insipidus
- Addison disease
- Primary lipodystrophy
- Acromegaly
Associations de patients 1
LEONA e.V. - Familienselbsthilfe bei seltenen chromosomalen Veränderungen
Kornblumenweg 38
59439
Holzwickede