Catalog

Rieger-Axenfeld anomaly

No MMS code

Link to WHO Definition

Rieger-Axenfeld anomaly – http://id.who.int/icd/entity/1338180594

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 (mild craniofacial dysmorphism, dental anomalies and redundant periumbilical skin).