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Pronunciation: glī-kol′ik as′i-dū′rē-ă
Definition: Excessive excretion of glycolic acid in the urine; a primary metabolic defect due to deficiency of 2-hydroxy-3-oxoadipate carboxylase, resulting in excretion of glycolic and oxalic acids, leading to the clinical syndrome of oxalosis.
Examples: glitazone, GI cocktail, etc.
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