Синдром Аксьонфельда-Рігера
ORPHA:782· ICD-10 Q13.8· Axenfeld-Rieger syndrome
Визначення(English summary)
Axenfeld-Rieger syndrome (ARS) is a generic term used to designate overlapping genetic disorders, in which the major physical condition is anterior segment dysgenesis of the eye. Patients with ARS may also present with multiple variable congenital anomalies.
- Поширеність
- 1-9 / 1 000 000
- Успадкування
- Autosomal dominant
- Вік початку
- Infancy, Neonatal