Beckwithův-Wiedemannův syndrom způsobený mutací CDKN1C
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation
- Dědičnost
- Autosomal dominant
- Věk nástupu
- Infancy, Neonatal
ORPHA:231120· ICD-10 Q87.3· Beckwith-Wiedemann syndrome due to CDKN1C mutation