Abstract
Hypoxanthine guanine phosphoribosyltransferase (HPRT) is a purine salvage enzyme responsible for the conversion of hypoxanthine and guanine to IMP and GMP, respectively. A deficiency of HPRT results in two distinct clinical disorders, gout (partial HPRT deficiency) or the Lesch-Nyhan syndrome (complete HPRT deficiency).1, 2
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