Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acid

J Pediatr. 1984 Jan;104(1):65-9. doi: 10.1016/s0022-3476(84)80591-0.

Abstract

An 8-month-old boy with severe lactic acidosis was found to have lipoamide dehydrogenase deficiency. Treatment with thiamine, biotin, bicarbonate, protein restriction, and ketogenic diet failed to alleviate the lactic acidosis. Oral administration of lipoic acid 25 to 50 mg/kg produced dramatic improvement in lactic and pyruvic acidemia, which has continued for 2 years and which has been accompanied by clinical improvement.

Publication types

  • Case Reports

MeSH terms

  • Acidosis / drug therapy*
  • Acidosis / urine
  • Administration, Oral
  • Dihydrolipoamide Dehydrogenase / deficiency*
  • Dihydrolipoamide Dehydrogenase / metabolism
  • Fibroblasts / enzymology
  • Humans
  • Infant
  • Ketoglutarate Dehydrogenase Complex / metabolism
  • Lactates*
  • Male
  • Pyruvate Dehydrogenase Complex / metabolism
  • Skin / cytology
  • Thioctic Acid / therapeutic use*

Substances

  • Lactates
  • Pyruvate Dehydrogenase Complex
  • Thioctic Acid
  • Ketoglutarate Dehydrogenase Complex
  • Dihydrolipoamide Dehydrogenase