Identification of a 220-kb insertion into the Duchenne gene in a family with an atypical course of muscular dystrophy

Genomics. 1989 May;4(4):592-6. doi: 10.1016/0888-7543(89)90283-8.

Abstract

Most known mutations in the gene region responsible for Duchenne or Becker muscular dystrophy are deletions of varying extent. Here we describe a 220-kb insertion within the DMD/BMD gene that cosegregates with a somewhat atypical course of muscular dystrophy in a pedigree. The insertion is demonstrated by field-inversion gel electrophoresis as an enlarged SfiI fragment hybridizing to probe J-Bir, while neighboring SfiI fragments (detected by probes PERT 87 and J-66) are unchanged. Hybridization with DMD c-DNA probes did not reveal alterations in coding sequences. In this pedigree, the altered SfiI fragments provide convenient markers for carrier identification.

Publication types

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

MeSH terms

  • Blotting, Southern
  • Child
  • DNA Mutational Analysis
  • DNA Probes
  • Electrophoresis, Agar Gel / methods
  • Female
  • Humans
  • Male
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophies / pathology
  • Pedigree
  • Polymorphism, Restriction Fragment Length

Substances

  • DNA Probes