Cardiac assessment in childhood carriers of Duchenne and Becker muscular dystrophies

Neuromuscul Disord. 2003 Feb;13(2):129-32. doi: 10.1016/s0960-8966(02)00197-9.

Abstract

Cardiac disease in adult female carriers of the X-linked dystrophinopathies, Duchenne and Becker muscular dystrophies, is a well-recognised entity. A single study has reported a 15% incidence of cardiac abnormalities in female carriers under 16 years. Our study aims, clinically and with electrocardiograph and echocardiograph, to determine the incidence of cardiac abnormality in young girls who are proven carriers of X-linked dystrophinopathies. Twenty-three girls aged 6.2-15.9 years were assessed. All had normal cardiac examination. None had electrocardiograph abnormalities consistent with dystrophic cardiomyopathy. Left ventricular fractional shortening ranged from 33 to 55% (normal>28%). Septal thickness, posterior wall thickness and wall thickness ratio were within normal limits. No cardiac abnormalities have been demonstrated in young girls who are proven carriers of X-linked dystrophinopathies in our study. This has important implications for planning timing of carrier determination and cardiac assessment.

Publication types

  • Comparative Study

MeSH terms

  • Adolescent
  • Child
  • Chromosomes, Human, X
  • Cross-Sectional Studies
  • Echocardiography / methods
  • Electroencephalography / methods
  • Female
  • Heart / physiopathology*
  • Heterozygote
  • Humans
  • Muscular Dystrophy, Duchenne / genetics
  • Muscular Dystrophy, Duchenne / physiopathology*