Succinyl-CoA:3-ketoacid transferase (SCOT) deficiency in a new patient homozygous for an R217X mutation

J Inherit Metab Dis. 2004;27(5):691-2. doi: 10.1023/b:boli.0000043023.57321.18.

Abstract

SCOT deficiency presents with persistent excess of ketones leading to ketoacidosis. Here we report patient GS15, homozygous for a novel R217X mutation, who had the first apparent ketoacidotic crisis at 8 months of age. Before confirmation of diagnosis, daily dialysis was the only mechanism by which to normalize her persistent metabolic acidosis of unknown aetiology.

Publication types

  • Case Reports

MeSH terms

  • Acidosis / genetics
  • Child, Preschool
  • Coenzyme A-Transferases / deficiency*
  • Coenzyme A-Transferases / genetics*
  • Consanguinity
  • Dialysis
  • Female
  • Homozygote
  • Humans
  • Mutation*
  • Time Factors

Substances

  • Coenzyme A-Transferases
  • 3-ketoacid CoA-transferase