Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp

Mov Disord. 2009 Jul 15;24(9):1390-2. doi: 10.1002/mds.22632.

Abstract

Task-specific focal upper limb dystonia can be part of the phenotypic spectrum of different types of hereditary dystonia. We investigated whether writer's cramp as presenting symptom is associated with mutations in DYT11, DYT16, or with the DYT1 GAG deletion in 43 patients. No DYT11 and DYT16 mutations were identified. One patient carried the GAG deletion in the DYT1 gene. In our cohort, writer's cramp as presenting symptom is not associated with mutations in DYT11, DYT16, but it can be the sole manifestation of DYT1 GAG deletion mutation carriers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Dystonic Disorders / genetics*
  • Female
  • Genetic Predisposition to Disease*
  • Genetic Testing / methods
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Molecular Chaperones / genetics*
  • Mutation / genetics*
  • RNA-Binding Proteins / genetics*
  • Sarcoglycans / genetics*
  • Trinucleotide Repeat Expansion / genetics
  • Young Adult

Substances

  • Molecular Chaperones
  • PRKRA protein, human
  • RNA-Binding Proteins
  • SGCE protein, human
  • Sarcoglycans
  • TOR1A protein, human