Very small dystrophin molecule in a family with a mild form of Becker dystrophy

Neuromuscul Disord. 1993 Jan;3(1):65-70. doi: 10.1016/0960-8966(93)90043-j.

Abstract

The genetic defect in a family with a mild form of Becker dystrophy was characterized by immunocytochemical, immunoblot and genomic DNA analysis in two patients and a carrier. Immunocytochemical localization on muscle preparations with a series of antibodies against different regions of the dystrophin molecule showed normal dystrophin expression with all the antibodies except anti-30 kDa antiserum. In the carrier's muscle, mosaicism was observed only with the anti-30 kDa. Immunoblot analysis revealed a band of about 250 kDa in the patients' muscles and a double band of normal and of reduced weight protein in carrier muscle. In the patients Multiplex-PCR (M-PCR) and Southern blot revealed deletions from exon 13 to exon 41. The study confirms that very mild Becker muscular dystrophy can be associated with a large intragenic deletion from the dystrophin gene.

Publication types

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

MeSH terms

  • Adult
  • Blotting, Southern
  • Child
  • DNA / blood
  • Dystrophin / analysis
  • Dystrophin / genetics*
  • Female
  • Genetic Carrier Screening*
  • Humans
  • Immunoblotting
  • Lymphocytes / metabolism
  • Male
  • Middle Aged
  • Molecular Weight
  • Muscles / pathology
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophies / pathology
  • Polymerase Chain Reaction

Substances

  • Dystrophin
  • DNA