Axenfeld-Rieger syndrome

MONDO:0019187

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.

Also known as: ARS, Axenfeld syndrome, Axenfeldt-Rieger syndrome, Rieger syndrome, goniodysgenesis hypodontia, iridogoniodysgenesis with somatic anomalies

14 clinical trials for this condition and its sub-types.

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