Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneity

Mov Disord. 2003 Sep;18(9):1047-51. doi: 10.1002/mds.10476.

Abstract

The epsilon-sarcoglycan gene (SGCE) on human chromosome 7q21 has been reported to be a major locus for inherited myoclonus-dystonia. Linkage to the SGCE locus has been detected in the majority of families tested, and mutations in the coding region have been found recently in families with autosomal dominant myoclonus-dystonia. To evaluate the relevance of SGCE in myoclonus-dystonia, we sequenced the entire coding region of the epsilon-sarcoglycan gene in 16 patients with either sporadic or familial myoclonus-dystonia. No mutations were found. This study suggests that epsilon-sarcoglycan does not play an important role in sporadic myoclonus-dystonia and supports genetic heterogeneity in familial cases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Cytoskeletal Proteins / analysis*
  • Cytoskeletal Proteins / genetics
  • Dystonic Disorders / genetics*
  • Female
  • Genetic Heterogeneity*
  • Humans
  • Male
  • Membrane Glycoproteins / analysis*
  • Membrane Glycoproteins / genetics
  • Middle Aged
  • Myoclonus / genetics*
  • Pedigree
  • Polymerase Chain Reaction
  • Sampling Studies
  • Sarcoglycans
  • Syndrome

Substances

  • Cytoskeletal Proteins
  • Membrane Glycoproteins
  • Sarcoglycans