Striking improvement of muscle strength under creatine therapy in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

J Inherit Metab Dis. 2003;26(1):67-8. doi: 10.1023/a:1024031714659.

Abstract

Creatine monohydrate given orally led to a long-lasting improvement of muscular weakness and ataxia in a girl with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Publication types

  • Case Reports

MeSH terms

  • 3-Hydroxyacyl CoA Dehydrogenases / deficiency*
  • Child
  • Creatine / therapeutic use*
  • Female
  • Humans
  • Lipid Metabolism, Inborn Errors / drug therapy*
  • Lipid Metabolism, Inborn Errors / physiopathology*
  • Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase
  • Muscle Weakness / drug therapy*
  • Muscle Weakness / etiology*
  • Muscle, Skeletal / physiopathology*
  • Recurrence
  • Rhabdomyolysis / etiology

Substances

  • 3-Hydroxyacyl CoA Dehydrogenases
  • Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase
  • Creatine