Sindrome di Beckwith-Wiedemann da deficit di CDKN1C
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation
- Trasmissione
- Autosomal dominant
- Età di esordio
- Infancy, Neonatal
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation