Clinical findings of a myoclonus-dystonia family with two distinct mutations

Neurology. 2002 Oct 22;59(8):1244-6. doi: 10.1212/wnl.59.8.1244.

Abstract

Myoclonus-dystonia has recently been associated with mutations in the epsilon-sarcoglycan gene (SCGE) on 7q21. Previously, the authors reported a patient with myoclonus-dystonia and an 18-bp deletion in the DYT1 gene on 9q34. The authors have now re-evaluated the patient harboring this deletion for mutations in the SGCE gene and identified a missense change. In the current study, the authors describe the clinical details of this family carrying mutations in two different dystonia genes. Further analysis of these mutations separately and together in cell culture and in animal models should clarify their functional consequences.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Carrier Proteins / genetics*
  • Cytoskeletal Proteins / genetics*
  • Dystonia / genetics*
  • Dystonia / psychology
  • Female
  • Humans
  • Male
  • Membrane Glycoproteins / genetics*
  • Middle Aged
  • Molecular Chaperones*
  • Mutation / genetics*
  • Myoclonus / genetics*
  • Myoclonus / psychology
  • Neuropsychological Tests
  • Pedigree
  • Sarcoglycans

Substances

  • Carrier Proteins
  • Cytoskeletal Proteins
  • Membrane Glycoproteins
  • Molecular Chaperones
  • Sarcoglycans
  • TOR1A protein, human