50 top medical experts on HPRT-Related Gout across 7 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- HPRT-Related Gout: Kelley-Seegmiller syndrome (KSS) is the mildest form of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency (see this term), a hereditary disorder of purine metabolism, and is associated with uric acid overproduction (UAO) leading to urolithiasis, and early-onset gout.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Partial HPRT Deficiency, Partial HPRT1 Deficiency, Partial Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency, Kelley-Seegmiller Syndrome
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