CDKN1C mutasyonuna bağlı Beckwith-Wiedemann sendromu
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation
- Kalıtım
- Autosomal dominant
- Başlangıç yaşı
- Infancy, Neonatal
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation