Hereditary Xanthinuria
- 1 January 1977
- journal article
- research article
- Published by S. Karger AG in Nephron
- Vol. 19 (6) , 328-332
- https://doi.org/10.1159/000180910
Abstract
Three patients with hereditary xanthinuria are presented and the pertinent literature is reviewed. In two siblings the disease has been asymptomatic; in the third urolithiasis has developed. Xanthine stone formation is the clinical hallmark of the disease. Hereditary xanthinuria seems to be relatively prevalent in Lebanon.Keywords
This publication has 3 references indexed in Scilit:
- Causes of HypouricemiaAnnals of Internal Medicine, 1973
- Hypouricemia due to Renal UricosuriaAnnals of Internal Medicine, 1973
- The Clinical Significance of HypouricemiaAnnals of Internal Medicine, 1973