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Ornithine translocase deficiency syndrome
Other Names for this Disease
- HHH syndrome
- Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
- Ornithine translocase 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.
Clinical Trials & Research for this Disease
- 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.