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ORPHA:91483· ICD-10 Q13.8· Rieger anomaly

Визначення(English summary)

Rieger's anomaly is a congenital ocular defect caused by anterior segment dysgenesis and is characterized by severe anterior chamber deformity with prominent strands and marked atrophy of the iris stroma, with hole or pseudo-hole formation and corectopia. The term covers the association of these iris and pupil anomalies with the features of Axenfeld’s anomaly (see this term).

Успадкування
Autosomal dominant
Вік початку
Neonatal