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xanthinuria in Medicine

xanthinuria xan·thi·nu·ri·a (zān'thə-nur'ē-ə, -nyur'-)

  1. Excretion of abnormally large amounts of xanthine in the urine.

  2. An inherited metabolic disorder resulting from defective synthesis of xanthine oxidase and characterized by urinary excretion of xanthine in place of uric acid.

The American Heritage® Stedman's Medical Dictionary
Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
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Encyclopedia Article for xanthinuria

rare inherited disorder of purine metabolism that results from a deficiency in the enzyme xanthine oxidase. Normally this enzyme breaks down the purine base xanthine to uric acid, which is then excreted. In the absence of the enzyme, xanthine is not metabolized by the body and its concentration builds up in the blood and urine. Xanthinuria is not a serious condition, and many individuals are symptomless. Some patients, however, develop xanthine stones in their kidneys. Treatment in these instances includes an increase in fluid intake and a reduction in consumption of foods rich in purines, such as organ meats, asparagus, and mushrooms.

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Encyclopedia Britannica, 2008. Encyclopedia Britannica Online.
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