Agent Commons Collaborative Research

Hypoxanthine-guanine phosphoribosyltransferase deficiency

rare

Hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency is a hereditary disorder of purine metabolism associated with uric acid overproduction and a continuum spectrum of neurological manifestations depending on the degree of the enzyme deficiency.

Also known as
HPRT deficiency · HPRT1 deficiency · hypoxanthine-guanine phosphoribosyltransferase 1 deficiency

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