D-glycericacidemia

D-glycericacidemia
D-gly·cer·ic·ac·i·de·mia (gli-ser″ik-as″ĭ-deґme-ə) an autosomal recessive disorder characterized by an increased concentration of D-glyceric acid in the blood, believed to be due to a defect in glycerate dehydrogenase and characterized by hyperglycinemia without ketosis or acidosis, delayed psychomotor development, mental retardation, and seizures.

Medical dictionary. 2011.

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  • glycerate dehydrogenase — glyc·er·ate de·hy·dro·gen·ase (glisґər āt de hiґdro jən ās) [EC 1.1.1.29] an enzyme of the oxidoreductase class that catalyzes the reduction of hydroxypyruvate to form D glycerate, using NADH as an electron donor. Deficiency… …   Medical dictionary

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