PAX6 gene
Overview Aniridia WAGR syndrome Anterior segment dysgenesis Microphthalmia, anophthalmia, coloboma (MAC) Additional information Clinical images References Overview Gene (OMIM No.)...
- Home
- Knowledge Base
- Axenfeld-Reiger anomaly
-
-
FOXC1 gene
Overview Axenfeld-Reiger anomaly Primary congenital glaucoma Peters anomaly References Overview Gene (OMIM No.) FOXC1 (#601090) Function of gene/protein Protein: Forkhead... -
Axenfeld-Rieger Anomaly (ARA) and Axenfeld-Rieger Syndrome (ARS): for professionals
Axenfeld-Reiger anomaly is a form of anterior segment dysgenesis with increased risk of glaucoma development. The main ocular feature is posterior embryotoxon. Other features include iris and pupil abnormalities. Axenfeld-Reiger syndrome is ARA with dental defect, craniofacial anomalies and redundant periumbilical skin.