Phenotypic variability in a Spanish family with a Caveolin-3 mutation

J Neurol Sci. 2009 Jan 15;276(1-2):95-8. doi: 10.1016/j.jns.2008.09.009. Epub 2008 Oct 19.

Abstract

We report a Spanish family affected from a late onset, hand-involved and autosomal dominant distal myopathy associated to Caveolin-3 mutation. Signs of muscle hyperexcitability and hyperckemia were observed in the youngest relatives but not motor symptoms.

Patients and methods: Neurological examination was performed in all members of the family. Muscle biopsy sample was taken from the proband and DNA genomics was amplified for the two exons of Cav-3 by the polymerase chain reaction (PCR) in all the affected members and in three asymptomatic relatives.

Results: Signs of muscle hyperexcitability and hyperckemia were observed in the affected members from early ages. Cav-3 expression was greatly reduced in the sarcolemma of the proband's muscle. Genetic studies revealed a G --> A transition at nucleotide position 80 in exon 1 of the Cav-3 gene (c.80G>A), generating a Arg --> Gln change at codon 27 (p.R27Q) of the amino acid chain in heterozygous state, while no mutation was found in unaffected members.

Conclusions: Signs of muscle hyperexcitability and hyperckemia at early ages may predict the development of a late onset autosomal dominant hand-involved myopathy associated to Cav-3 mutation in the family reported herein.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Arginine / genetics
  • Caveolin 3 / genetics*
  • Caveolin 3 / metabolism
  • DNA Mutational Analysis / methods
  • Distal Myopathies / genetics*
  • Distal Myopathies / pathology
  • Distal Myopathies / physiopathology
  • Exons / genetics
  • Family Health*
  • Glycine / genetics
  • Humans
  • Male
  • Muscle, Skeletal / pathology
  • Muscle, Skeletal / ultrastructure
  • Mutation / genetics*
  • Neurologic Examination / methods
  • Phenotype*
  • Spain

Substances

  • Caveolin 3
  • Arginine
  • Glycine