glycolic aciduria

gly·col·ic ac·i·du·ri·a

(glī-kol'ik as'i-dū'rē-ă),
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.

gly·col·ic ac·i·du·ri·a

(glī-kol'ik as'i-dyūr'ē-ă)
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.
References in periodicals archive ?
Persistent glycolic aciduria in a healthy child with normal alanine-glyoxylate aminotransferase activity.