Sporadic rapid‐onset dystonia–parkinsonism syndrome: Failure of bilateral pallidal stimulation
Identifieur interne : 002130 ( Istex/Checkpoint ); précédent : 002129; suivant : 002131Sporadic rapid‐onset dystonia–parkinsonism syndrome: Failure of bilateral pallidal stimulation
Auteurs : Angela Deutschl Nder [Allemagne] ; Friedrich Asmus [Allemagne] ; Thomas Gasser [Allemagne] ; Ulrich Steude [Allemagne] ; Kai Bötzel [Allemagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2005-02.
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- KwdEn :
Abstract
We report on a woman who had a severe sporadic nonprogressive dystonia–parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid‐onset dystonia–parkinsonism, except for autosomal‐dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms. © 2004 Movement Disorder Society
Url:
DOI: 10.1002/mds.20296
Affiliations:
- Allemagne
- Bade-Wurtemberg, Bavière, District de Haute-Bavière, District de Tübingen
- Munich, Tübingen
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<series><title level="j">Movement Disorders</title>
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<front><div type="abstract" xml:lang="en">We report on a woman who had a severe sporadic nonprogressive dystonia–parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid‐onset dystonia–parkinsonism, except for autosomal‐dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms. © 2004 Movement Disorder Society</div>
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