Sporadic rapid‐onset dystonia–parkinsonism syndrome: Failure of bilateral pallidal stimulation
Identifieur interne : 003724 ( Main/Curation ); précédent : 003723; suivant : 003725Sporadic 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.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Adult, Dystonia, Dystonic Disorders (complications), Dystonic Disorders (therapy), Electric Stimulation Therapy, Female, Globus Pallidus (physiopathology), Globus Pallidus (radiation effects), Humans, Motor control, Nervous system diseases, Parkinsonian Disorders (complications), Parkinsonian Disorders (therapy), Parkinsonism, Severity of Illness Index, Sporadic, 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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<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Sporadic rapid‐onset dystonia–parkinsonism syndrome: Failure of bilateral pallidal stimulation</title>
<author><name sortKey="Deutschl Nder, Angela" sort="Deutschl Nder, Angela" uniqKey="Deutschl Nder A" first="Angela" last="Deutschl Nder">Angela Deutschl Nder</name>
<affiliation wicri:level="3"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurology, Klinikum Grosshadern, Ludwig‐Maximilians University, Munich</wicri:regionArea>
<placeName><region type="land" nuts="1">Bavière</region>
<region type="district" nuts="2">District de Haute-Bavière</region>
<settlement type="city">Munich</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Asmus, Friedrich" sort="Asmus, Friedrich" uniqKey="Asmus F" first="Friedrich" last="Asmus">Friedrich Asmus</name>
<affiliation wicri:level="3"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurodegenerative Diseases, Hertie‐Institute for Clinical Brain Research, University of Tübingen, Tübingen</wicri:regionArea>
<placeName><region type="land" nuts="1">Bade-Wurtemberg</region>
<region type="district" nuts="2">District de Tübingen</region>
<settlement type="city">Tübingen</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Gasser, Thomas" sort="Gasser, Thomas" uniqKey="Gasser T" first="Thomas" last="Gasser">Thomas Gasser</name>
<affiliation wicri:level="3"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurodegenerative Diseases, Hertie‐Institute for Clinical Brain Research, University of Tübingen, Tübingen</wicri:regionArea>
<placeName><region type="land" nuts="1">Bade-Wurtemberg</region>
<region type="district" nuts="2">District de Tübingen</region>
<settlement type="city">Tübingen</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Steude, Ulrich" sort="Steude, Ulrich" uniqKey="Steude U" first="Ulrich" last="Steude">Ulrich Steude</name>
<affiliation wicri:level="3"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurosurgery, Klinikum Grosshadern, Ludwig‐Maximilians University, Munich</wicri:regionArea>
<placeName><region type="land" nuts="1">Bavière</region>
<region type="district" nuts="2">District de Haute-Bavière</region>
<settlement type="city">Munich</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Botzel, Kai" sort="Botzel, Kai" uniqKey="Botzel K" first="Kai" last="Bötzel">Kai Bötzel</name>
<affiliation wicri:level="3"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurology, Klinikum Grosshadern, Ludwig‐Maximilians University, Munich</wicri:regionArea>
<placeName><region type="land" nuts="1">Bavière</region>
<region type="district" nuts="2">District de Haute-Bavière</region>
<settlement type="city">Munich</settlement>
</placeName>
</affiliation>
</author>
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<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2005-02">2005-02</date>
<biblScope unit="vol">20</biblScope>
<biblScope unit="issue">2</biblScope>
<biblScope unit="page" from="254">254</biblScope>
<biblScope unit="page" to="257">257</biblScope>
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<idno type="DOI">10.1002/mds.20296</idno>
<idno type="ArticleID">MDS20296</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Dystonic Disorders (complications)</term>
<term>Dystonic Disorders (therapy)</term>
<term>Electric Stimulation Therapy</term>
<term>Female</term>
<term>Globus Pallidus (physiopathology)</term>
<term>Globus Pallidus (radiation effects)</term>
<term>Humans</term>
<term>Parkinsonian Disorders (complications)</term>
<term>Parkinsonian Disorders (therapy)</term>
<term>Severity of Illness Index</term>
<term>bilateral deep brain stimulation</term>
<term>globus pallidus</term>
<term>rapid‐onset dystonia–parkinsonism</term>
<term>severe sporadic nonprogressive dystonia–parkinsonism syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Dystonic Disorders</term>
<term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Globus Pallidus</term>
</keywords>
<keywords scheme="MESH" qualifier="radiation effects" xml:lang="en"><term>Globus Pallidus</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Dystonic Disorders</term>
<term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Electric Stimulation Therapy</term>
<term>Female</term>
<term>Humans</term>
<term>Severity of Illness Index</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
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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>
</front>
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