Reports

Urinary Metabolites in Congenital Hyperuricosuria

+ See all authors and affiliations

Science  26 May 1967:
Vol. 156, Issue 3778, pp. 1122-1123
DOI: 10.1126/science.156.3778.1122

Abstract

The excretion of oxypurine metabolites in urine of patients with congenital hyperuricosuria exceeds, on a creatinine basis, that observed in any previously recognized metabolic anomaly. The ratio of hypoxanthine to xanthine is from 2:1 to 3:1 and results from increased hypoxanthine excretion, in contrast to other hyperuricosuric conditions where ratios of less than one have been reported. Administration of allopurinol (a xanthine-oxidase inhibitor) reduces the excretion of uric acid but results in an equivalent increase in xanthine and hypoxanthine. These features appear to be unique to congenital hyper-uricosuria.

Related Content