L-Glyceric aciduria

Rashed, M.S. et al., Chiral liquid chromatography tandem mass spectrometry in the determination of the configurations of glyceric acid in urine of patients with D-glyceric and L-glyceric acidurias, Biomed. Chromatogr, 16, 191, 2002. [Pg.167]

L-glyceric aciduria (Primary hyperoxaluria Type II) L-glyceric, oxalic... [Pg.63]

Calcium oxalate kidney stones L-glyceric aciduria... [Pg.231]

L-glyceric aciduria urinary excretion of oxalic acid, urinary L-glyceric acid oxalate stones D-glyceric dehydrogenase deficiency Autosomal recessive Williams, H.E., and Smith, L.H., Jr. L-glyceric aciduria a new genetic variant of primary hyperoxaluria. N. Engl. J. Med. 278, 233-239 (1968)... [Pg.232]

Recently, inherited metabolic diseases have been described in which a particular enantiomeric form of a metabolite is exclusively excreted [42]. Typical examples are D(-l-)-glyceric aciduria [43] and L-2-hydroxyglutaric aciduria [44], Using conventional GC-MS for urinary organic acid screening, increased amounts of these... [Pg.349]

Type II (L-glyceric aciduria) L-glyceric and oxalic acids D-Glycerate dehydrogenase (EC 1.1.1.29) (glyoxylate reductase) 16.3.2... [Pg.219]

Williams, H.E. and Smith, L.H. (1971), Hyperoxaluria in L-glyceric aciduria Possible pathogenic mechanism. Science, 171,390. [Pg.444]

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