Iridogoniodysgenesis type 1
Other Names for this Disease
- Iridogoniodysgenesis anomaly, Autosomal dominant
- IGDA syndrome
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.
iris (the colored part of the eye) and cornea, which eventually lead to early-onset glaucoma. The irides of affected people are unusually dark. For example, studies of the condition often describe 'brown' irides as a dark, chocolate color and 'blue' irides as a very dark, slate gray. The iris also lacks the usual pattern and has a smooth appearance. Iridogoniodysgenesis type 1 is caused by changes (mutations) in the FOXC1 gene and is inherited in an autosomal dominant manner. Management is based on the signs and symptoms present in each person and is generally focused on the screening and eventual treatment of glaucoma.Iridogoniodysgenesis type 1 is a rare condition that affects the eyes. People with this condition are born with malformations of the
Last updated: 3/22/2016
- Iridogoniodysgenesis, Type 1. University of Arizona College of Medicine, Department of Ophthalmology and Vision Science. http://disorders.eyes.arizona.edu/disorders/iridogoniodysgenesis-type-1. Accessed 3/22/2016.
- IRIDOGONIODYSGENESIS, TYPE 1. OMIM. March 2011; http://www.omim.org/entry/601631.
On this page
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Iridogoniodysgenesis type 1. Click on the link to view a sample search on this topic.