Sporadic rapid‐onset dystonia–parkinsonism syndrome: Failure of bilateral pallidal stimulation
Identifieur interne : 004E07 ( Main/Merge ); précédent : 004E06; suivant : 004E08Sporadic 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.
English descriptors
- KwdEn :
- Adult, Dystonic Disorders (complications), Dystonic Disorders (therapy), Electric Stimulation Therapy, Female, Globus Pallidus (physiopathology), Globus Pallidus (radiation effects), Humans, Parkinsonian Disorders (complications), Parkinsonian Disorders (therapy), Severity of Illness Index, bilateral deep brain stimulation, globus pallidus, rapid‐onset dystonia–parkinsonism, severe sporadic nonprogressive dystonia–parkinsonism syndrome.
- MESH :
- complications : Dystonic Disorders, Parkinsonian Disorders.
- physiopathology : Globus Pallidus.
- radiation effects : Globus Pallidus.
- therapy : Dystonic Disorders, Parkinsonian Disorders.
- Adult, Electric Stimulation Therapy, Female, Humans, Severity of Illness Index.
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
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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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<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.</div>
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