Syndrome de Beckwith-Wiedemann dû à une mutation de CDKN1C
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation
- Transmission
- Autosomal dominant
- Âge de début
- Infancy, Neonatal
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation