Lesch-Nyhan syndrome overview: Difference between revisions
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Created page with "{{Lesch-Nyhan syndrome}} {{CMG}}; {{AE}} {{AN}} ==Overview== '''Lesch-Nyhan's syndrome''', is a rare, inherited disorder caused by a deficiency of the enzyme [[hypoxa..." |
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Revision as of 03:40, 28 August 2012
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Lesch-Nyhan syndrome Microchapters |
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Lesch-Nyhan syndrome overview On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aarti Narayan, M.B.B.S [2]
Overview
Lesch-Nyhan's syndrome, is a rare, inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT).