Fortuitous Discovery of Hereditary Xanthinuria.

ola Kala shared this article with you from Inoreader Fortuitous Discovery of Hereditary Xanthinuria. Μέσω pubmed: "clin lab"[jour] Fortuitous Discovery of Hereditary Xanthinuria. Clin Lab. 2020 Oct 01;66(10): Authors: Biaz A, Tazi S, Bouhsain S, Chemsi M, Dami A, Machtani-Idrissi SE Abstract Hereditary xanthinuria was the first inherited purine metabolism disorder described. It is a rare pathology, which is most often asymptomatic and whose incidence is therefore underestimated. We report the case of a patient with an undetectable level of uric acid in the blood, discovered during a systematic biological assessment. This case report recalls the existence of this rare metabolic disorder, which is usually benign, but can lead to complications, and the importance of considering an abnormality of the purine cycle when discovering a hypo-uricemia. PMID: 33073950 [PubMed - in process] View on the web Inoreader. Take back control of your news feed. Follow us on Twitter and Facebook.