[Late diagnosis of a McArdle disease's case (type V glycogenosis)]

Ann Biol Clin (Paris). 2007 Sep-Oct;65(5):550-4.
[Article in French]

Abstract

McArdle's disease is a metabolic myopathy characterized by a myophosphorylase deficiency resulting in an inability to degrade glycogen stores. We report the case of a 48 years old patient who complained since adolescence of rest and exercise myalgias and presented a chronic increased plasma creatine kinase activity. First, a maximal exercise test was performed. This test demonstrated a quasi lack of rise of respiratory exchange ratio and of blood lactate, possibly due to a glycogenolytic/glycolytic pathway deficiency. Second, a biopsy of vastus lateralis muscle was performed using Bergström needle. As expected, the analysis of mitochondrial function was normal. The in vitro screening test of the glycogenolysis/glycolysis pathway showed a lack of lactate production in presence of glycogen substrate. The study of muscular metabolism of glycogen revealed a glycogen accumulation and a decrease of active and total phosphorylase activities. These data allowed us to diagnose a type V glycogenosis, or McArdle's disease. The patient appeared heterozygous for the most frequent mutation (p.R50X).

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Creatine Kinase / blood
  • Exercise Test
  • Female
  • Glycogen / metabolism
  • Glycogen Phosphorylase, Muscle Form / genetics
  • Glycogen Storage Disease Type V / diagnosis*
  • Glycogen Storage Disease Type V / genetics
  • Heterozygote
  • Humans
  • Lactic Acid / blood
  • Middle Aged
  • Muscle, Skeletal / metabolism
  • Mutation / genetics
  • Phosphorylases / analysis
  • Pulmonary Gas Exchange

Substances

  • Lactic Acid
  • Glycogen
  • Glycogen Phosphorylase, Muscle Form
  • Phosphorylases
  • Creatine Kinase