Gyrate atrophy of choroid and retina
Other Names for this Disease
- Ornithine aminotransferase deficiency
- Ornithine ketoacid aminotransferase deficiency
- Gyrate atrophy
- OAT deficiency
- OKT deficiency
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- GeneReviews provides a current, expert-authored, peer-reviewed, full-text article urea cycle disorders in general that you may find helpful. GeneReview articles describe the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions.
- ClinicalTrials.gov lists trials that are studying or have studied Gyrate atrophy of choroid and retina. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.
- The U.S. National Institutes of Health, through the National Library of Medicine, developed ClinicalTrials.gov to provide patients, family members, and members of the public with current information on clinical research studies. There is a study titled Study of Treatment and Metabolism in Patients With Urea Cycle Disorders which may be of interest to you. To find this trial, click on the link above.
- The Section on Ophthalmic Clinical Genetics research group at the National Eye Institute has been a leader in studying gyrate atrophy of the choroid and retina and nephropathic cystinosis. You can read more about this group by clicking on the link above.
- Orphanet lists European clinical trials, research studies, and patient registries enrolling people with this condition.