Sindrome di Pierre Robin - anomalia faciodigitale
ORPHA:2888· ICD-10 Q87.8· Pierre Robin syndrome-faciodigital anomaly syndrome
- Prevalenza
- <1 / 1 000 000
- Trasmissione
- X-linked recessive
- Età di esordio
- Infancy, Neonatal
ORPHA:2888· ICD-10 Q87.8· Pierre Robin syndrome-faciodigital anomaly syndrome