Microstructural white matter changes in carriers of the DYT1 gene mutation. Academic Article uri icon

Overview

abstract

  • We tested the hypothesis that the DYT1 genotype is associated with a disorder of anatomical connectivity involving primarily the sensorimotor cortex. We used diffusion tensor magnetic resonance imaging (DTI) to assess the microstructure of white matter pathways in mutation carriers and control subjects. Fractional anisotropy (FA), a measure of axonal integrity and coherence, was reduced (p < 0.005) in the subgyral white matter of the sensorimotor cortex of DYT1 carriers. Abnormal anatomical connectivity of the supplementary motor area may contribute to the susceptibility of DYT1 carriers to develop clinical manifestations of dystonia.

publication date

  • August 1, 2004

Research

keywords

  • Cerebral Cortex
  • Dystonia
  • Genetic Predisposition to Disease
  • Molecular Chaperones
  • Mutation

Identity

Scopus Document Identifier

  • 3843067672

Digital Object Identifier (DOI)

  • 10.1002/ana.20177

PubMed ID

  • 15293281

Additional Document Info

volume

  • 56

issue

  • 2