Polymalformative genetic syndrome with increased risk of developing cancer
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Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
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- Noonan syndrome
- Li-Fraumeni syndrome
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Familial ovarian cancer
- Inherited cancer-predisposing syndrome
- Hereditary retinoblastoma
- Constitutional mismatch repair deficiency syndrome
- Von Hippel-Lindau disease
- Full NF2-related schwannomatosis
- Silver-Russell syndrome
- Hereditary nonpolyposis colon cancer
- Common variable immunodeficiency
- Diamond-Blackfan anemia
- Ataxia-telangiectasia
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
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- Xeroderma pigmentosum
- Familial ovarian cancer
- Beckwith-Wiedemann syndrome
- Cockayne syndrome
- Von Hippel-Lindau disease
- Costello syndrome
- Maffucci syndrome
- Noonan syndrome
- Silver-Russell syndrome
- APC-related attenuated familial adenomatous polyposis
- Ataxia-telangiectasia
- Diamond-Blackfan anemia
- Full NF2-related schwannomatosis
- Li-Fraumeni syndrome
- Inherited renal cancer-predisposing syndrome