Синдром Фрімана-Шелдона
ORPHA:2053· ICD-10 Q87.0· Freeman-Sheldon syndrome
Визначення(English summary)
A rare congenital, distal arthogryposis syndrome characterized by microstomia, whistling-face appearance, Chin with V- or H- shaped creased, and prominent nasolabial folds; most patients present club foot and congenital joint contractures of the hands and feet. It is the most severe form of distal arthrogryposis.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Autosomal dominant, Autosomal recessive
- Вік початку
- Antenatal, Neonatal