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[sis-tuh-noo r-ee-uh, -nyoo r-] /ˌsɪs təˈnʊər i ə, -ˈnyʊər-/
noun, Pathology.
an inherited metabolic disorder that results in the excessive excretion of certain amino acids, especially cystine, in the urine.
Origin of cystinuria
First recorded in 1850-55; cystine + -uria Unabridged
Based on the Random House Dictionary, © Random House, Inc. 2018.
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cystinuria in Medicine

cystinuria cys·ti·nu·ri·a (sĭs'tə-nur'ē-ə, -nyur'-)
A hereditary condition characterized by excessive urinary excretion of cystine, lysine, arginine, and ornithine, caused by a defect in the renal tubules that impairs reabsorption of these acids.

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