Primary hyperoxaluria type 1
Other Names for this Disease
- Alanine-glyoxylate aminotransferase deficiency
- Glycolic aciduria
- Hepatic AGT deficiency
- Oxalosis 1
- GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions. Click on the link to view the article on this topic.
- ClinicalTrials.gov lists trials that are studying or have studied Primary hyperoxaluria type 1. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.