Ailesel sikafosefali sendromu, McGillivray tipi
ORPHA:168624· ICD-10 Q87.0· Familial scaphocephaly syndrome, McGillivray type
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal dominant
- Başlangıç yaşı
- Infancy, Neonatal
ORPHA:168624· ICD-10 Q87.0· Familial scaphocephaly syndrome, McGillivray type