Molecular characterization of McArdle's disease in two large Finnish families

J Neurol Sci. 1999 Jun 1;165(2):121-5. doi: 10.1016/s0022-510x(99)00091-x.

Abstract

We have studied two large unrelated Finnish families with myophosphorylase deficiency (McArdle's disease). In one, we identified a new nonsense mutation at codon 540 in exon 14 of the myophosphorylase gene, changing an encoded glutamic acid to a stop codon (E540X). The second family carried a splice-junction mutation at the 5' splice site of intron 14 (1844+G-->A), previously reported in one Caucasian patient and in a consanguineous Druze family. These data further enlarge the list of mutations associated with McArdle's disease and establish that McArdle's disease is genetically heterogeneous also within the Finnish population.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Codon, Nonsense
  • DNA / genetics
  • Female
  • Finland
  • Glycogen Storage Disease Type V / genetics*
  • Glycogen Storage Disease Type V / metabolism
  • Glycogen Storage Disease Type V / pathology
  • Humans
  • Muscle, Skeletal / pathology
  • Mutation
  • Pedigree
  • Phosphorylases / deficiency
  • Phosphorylases / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Trans-Splicing

Substances

  • Codon, Nonsense
  • DNA
  • Phosphorylases