Diagnosis of X-linked Emery-Dreifuss muscular dystrophy by protein analysis of leucocytes and skin with monoclonal antibodies

Neuromuscul Disord. 1997 Jan;7(1):63-6. doi: 10.1016/s0960-8966(96)00405-1.

Abstract

The X-linked form of Emery-Dreifuss muscular dystrophy (EDMD) was recently shown to be due to mutations in the STA gene on chromosome Xq28. We have demonstrated a simple test for the diagnosis of this condition, looking for altered expression of the protein, emerin, in leucocytes and skin with a monoclonal antibody. Full-length emerin is completely absent in affected boys from the EDMD families studied. The method has also enabled identification of a female carrier of the disease by reduced levels of the protein on the leucocyte Western blot and a mosaic pattern of expression by immunofluorescence microscopy of the skin biopsy.

Publication types

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

MeSH terms

  • Adolescent
  • Antibodies, Monoclonal
  • Female
  • Fluorescent Antibody Technique
  • Genetic Carrier Screening
  • Genetic Linkage*
  • Humans
  • Immunologic Tests*
  • Leukocytes / metabolism*
  • Male
  • Membrane Proteins / metabolism*
  • Muscular Dystrophies / diagnosis*
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophy, Emery-Dreifuss
  • Nuclear Proteins
  • Pedigree
  • Skin / metabolism*
  • Thymopoietins / metabolism*
  • X Chromosome*

Substances

  • Antibodies, Monoclonal
  • Membrane Proteins
  • Nuclear Proteins
  • Thymopoietins
  • emerin