D-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. 

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)... 

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... 

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

Fig. 16.2 Chromatogram of organic acids extracted using ethyl acetate and diethyl ether from the urine of a patient with o-glyceric aciduria (Brandt et al, 1976) and separated as their trimethylsiiyl derivatives on 3 per cent OV-1. Peak identifications are 1, glycollate plus lactate 2, urea 3, glycerate (d) 4, 4-hydroxyphenylacetate. (Redrawn with modifications from Brandt et al, 1976)...

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