Beckwith-Wiedemann-Syndrom durch CDKN1C-Mangel
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- Infancy, Neonatal
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation