Isolated hemihyperplasia
All Entries 4
Zentrum für Gefäßfehlbildungen am Universitätsklinikum Freiburg
Universitätsklinikum Freiburg Freiburg Zentrum für Seltene Erkrankungen (FZSE)
Breisacher Str. 62
79106 Freiburg
0761 27043021
0761 2709643366
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Email
- Facial arteriovenous malformation
- Beckwith-Wiedemann syndrome
- Macrocystic lymphatic malformation
- Dural sinus malformation
- Von Hippel-Lindau disease
- Rare venous malformation
- Primary lymphedema
- Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome
- Vein of Galen aneurysmal malformation
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
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Email
- Inherited cancer-predisposing syndrome
- Silver-Russell syndrome
- Full NF2-related schwannomatosis
- Diamond-Blackfan anemia
- Li-Fraumeni syndrome
- Familial ovarian cancer
- Common variable immunodeficiency
- Hereditary retinoblastoma
- Ataxia-telangiectasia
- Constitutional mismatch repair deficiency syndrome
- Von Hippel-Lindau disease
- Xeroderma pigmentosum
- Noonan syndrome
- Beckwith-Wiedemann syndrome
- Hereditary nonpolyposis colon cancer
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Page Web
Email
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Li-Fraumeni syndrome
- Noonan syndrome
- Maffucci syndrome
- Familial ovarian cancer
- Cockayne syndrome
- Ataxia-telangiectasia
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Diamond-Blackfan anemia
- Inherited renal cancer-predisposing syndrome
- Silver-Russell syndrome
- Von Hippel-Lindau disease
- Costello syndrome
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
- Inherited cancer-predisposing syndrome
- Silver-Russell syndrome
- Full NF2-related schwannomatosis
- Diamond-Blackfan anemia
- Li-Fraumeni syndrome
- Familial ovarian cancer
- Common variable immunodeficiency
- Hereditary retinoblastoma
- Ataxia-telangiectasia
- Constitutional mismatch repair deficiency syndrome
- Von Hippel-Lindau disease
- Xeroderma pigmentosum
- Noonan syndrome
- Beckwith-Wiedemann syndrome
- Hereditary nonpolyposis colon cancer
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Page Web
Email
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Li-Fraumeni syndrome
- Noonan syndrome
- Maffucci syndrome
- Familial ovarian cancer
- Cockayne syndrome
- Ataxia-telangiectasia
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Diamond-Blackfan anemia
- Inherited renal cancer-predisposing syndrome
- Silver-Russell syndrome
- Von Hippel-Lindau disease
- Costello syndrome
Institutions de prise en charge 1
Zentrum für Gefäßfehlbildungen am Universitätsklinikum Freiburg
Universitätsklinikum Freiburg Freiburg Zentrum für Seltene Erkrankungen (FZSE)
Breisacher Str. 62
79106 Freiburg
0761 27043021
0761 2709643366
Page Web
Email
- Facial arteriovenous malformation
- Beckwith-Wiedemann syndrome
- Macrocystic lymphatic malformation
- Dural sinus malformation
- Von Hippel-Lindau disease
- Rare venous malformation
- Primary lymphedema
- Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome
- Vein of Galen aneurysmal malformation