Effect of thalamotomy on focal hand dystonia in a family with DYT1 mutation
Identifieur interne : 001438 ( Istex/Checkpoint ); précédent : 001437; suivant : 001439Effect of thalamotomy on focal hand dystonia in a family with DYT1 mutation
Auteurs : Mi J. Kim [Corée du Sud] ; Sang R. Jeon [Corée du Sud] ; Han-Wook Yoo [Corée du Sud] ; Gu-Hwan Kim [Corée du Sud] ; Myoung C. Lee [Corée du Sud] ; Sun J. Chung [Corée du Sud]Source :
- Movement Disorders [ 0885-3185 ] ; 2008-11-15.
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Abstract
We report the clinical and molecular features of a family with focal hand dystonia caused by DYT1 mutation. Four members of a family who underwent thalamotomy showed a marked and sustained therapeutic benefit that lasted for up to 12 years without recurrence of dystonia or any significant surgical complication. The hand dystonia caused by DYT1 mutation may be successfully managed by thalamotomy. © 2008 Movement Disorder Society
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DOI: 10.1002/mds.22337
Affiliations:
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<front><div type="abstract" xml:lang="en">We report the clinical and molecular features of a family with focal hand dystonia caused by DYT1 mutation. Four members of a family who underwent thalamotomy showed a marked and sustained therapeutic benefit that lasted for up to 12 years without recurrence of dystonia or any significant surgical complication. The hand dystonia caused by DYT1 mutation may be successfully managed by thalamotomy. © 2008 Movement Disorder Society</div>
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