Síndrome de Beckwith-Wiedemann por una mutación en el gen CDKN1C
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation
- Herencia
- Autosomal dominant
- Edad de inicio
- Infancy, Neonatal
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation