A family of Emery-Dreifuss muscular dystrophy with extreme difference in severity

Pediatr Neurol. 2005 May;32(5):358-60. doi: 10.1016/j.pediatrneurol.2004.12.011.

Abstract

This report describes two patients, a father and son, with autosomal dominant Emery-Dreifuss muscular dystrophy. Although the father had the common phenotype, the son had a severe phenotype including early onset of weakness and fatal cardiomyopathy in childhood. Among the patients with severe phenotype of autosomal dominant Emery-Dreifuss muscular dystrophy, he is the first to have familial onset, and in the severe end of this disease spectrum.

Publication types

  • Case Reports

MeSH terms

  • Brain / pathology
  • Child
  • Child, Preschool
  • Family Health
  • Genes, Dominant
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Muscular Dystrophy, Emery-Dreifuss / genetics*
  • Muscular Dystrophy, Emery-Dreifuss / pathology
  • Muscular Dystrophy, Emery-Dreifuss / physiopathology*
  • Pedigree
  • Phenotype
  • Severity of Illness Index