L-2-Hydroxyglutaric aciduria: an inborn error of metabolism?

J Inherit Metab Dis. 1980;3(4):109-12. doi: 10.1007/BF02312543.

Abstract

A 5-year-old boy, excreting large amounts of 2-hydroxyglutaric acid in the urine (3.3-7.6 mmol/l), is described. The patient presented with psychomotor retardation and dystrophy. His skeletal age was delayed. The EEG was not well differentiated; it resembled that observed in 2-year-old children. There was a severe anaemia, which reacted well to iron supplements. The 2-hydroxyglutaric acid was found to have the L-configuration, as analysed by capillary gas chromatography of the O-acetylated di-(-)-2-butyl ester derivative. The relation of L-2-hydroxyglutarate excretion to known metabolic pathways is discussed.

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Glutarates / metabolism
  • Glutarates / urine*
  • Humans
  • Hydroxy Acids / metabolism
  • Hydroxy Acids / urine
  • Ketoglutaric Acids / metabolism
  • Ketoglutaric Acids / urine
  • Male
  • Metabolism, Inborn Errors / metabolism
  • Metabolism, Inborn Errors / urine*

Substances

  • Glutarates
  • Hydroxy Acids
  • Ketoglutaric Acids
  • alpha-hydroxyglutarate