Síndrome de Beckwith-Wiedemann por deficiência no gene CDKN1C
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation
- Hereditariedade
- Autosomal dominant
- Idade de início
- Infancy, Neonatal
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation