l-glyceric aciduria

l-gly·cer·ic ac·i·dur·i·a

(gli-sĕr'ik as'i-dūr'ē-ă),
Excretion of l-glyceric acid in the urine; a primary metabolic error due to deficiency of d-glyceric dehydrogenase resulting in excretion of l-glyceric and oxalic acids, leading to the clinical syndrome of oxalosis with frequent formation of oxalate renal calculi.

l-gly·cer·ic ac·id·u·ri·a

(glī-ser'ik as'i-dyūr'ē-ă)
Excretion of l-glyceric acid in the urine; a primary metabolic error due to deficiency of d-glyceric dehydrogenase, resulting in excretion of l-glyceric and oxalic acids and leading to the clinical syndrome of oxalosis with frequent formation of oxalate renal calculi.
References in periodicals archive ?
L-Glyceric aciduria: a new genetic variant of primary hyperoxaluria.
Primary oxaluria type II (L-glyceric aciduria): a rare cause of nephrolithiasis in children.
Extraction of glyceric and glycolic acids from urine with tetrahydrofuran: utility in detection of primary hyperoxaluria
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