Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency

Neuromuscul Disord. 2012 Aug;22(8):685-9. doi: 10.1016/j.nmd.2012.05.006. Epub 2012 Jun 22.

Abstract

The aim of this retrospective study was to assess respiratory and cardiac function in a large cohort of patients with congenital muscular dystrophies (CMD) with reduced glycosylation of alphadystroglycan (α-DG). Thirteen of the 115 patients included in the study died between the age of 1 month and 20 years. The age at last follow up of the surviving 102 ranged between 1 year and 68 years (median: 9.3 years). Cardiac involvement was found in 7 of the 115 (6%), 5 with dilated cardiomyopathy, 1 cardiac conductions defects and 1 mitral regurgitation. Respiratory function was impaired in 14 (12%). Ten of the 14 required non invasive nocturnal respiratory support, while the other four required invasive ventilation. Cardiac or respiratory involvement was found in patients with mutations in FKRP, POMT1, POMT2. All of the patients in whom mutation in POMGnT1 were identified had normal cardiac and respiratory function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Brain / pathology
  • Cardiomyopathy, Dilated / epidemiology
  • Child
  • Child, Preschool
  • Cohort Studies
  • Dystroglycans / deficiency*
  • Dystroglycans / metabolism
  • Follow-Up Studies
  • Heart / physiopathology*
  • Humans
  • Incidence
  • Infant
  • Infant, Newborn
  • Magnetic Resonance Imaging
  • Mannosyltransferases / genetics
  • Middle Aged
  • Mitral Valve Insufficiency / epidemiology
  • Muscular Dystrophies / congenital*
  • Muscular Dystrophies / genetics
  • Muscular Dystrophies / physiopathology*
  • Mutation / genetics
  • Pentosyltransferases
  • Proteins / genetics
  • Respiratory System / physiopathology*
  • Retrospective Studies
  • Ventilators, Mechanical
  • Young Adult

Substances

  • Proteins
  • Dystroglycans
  • Mannosyltransferases
  • protein O-mannosyltransferase
  • FKRP protein, human
  • Pentosyltransferases