Синдром Пая
ORPHA:1993· ICD-10 Q87.8· Pai syndrome
Визначення(English summary)
A rare frontonasal dysplasia characterized by median cleft of the upper lip (MCL), midline polyps of the facial skin, nasal mucosa, and pericallosal lipomas. Hypertelorism with ocular anomalies are also observed, generally with normal neuropsychological development.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Unknown
- Вік початку
- Antenatal, Neonatal