Phenotypic spectrum of musician's dystonia: A task‐specific disorder?
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Auteurs : Alexander Schmidt [Allemagne] ; Hans-Christian Jabusch [Allemagne] ; Eckart Altenmüller [Allemagne] ; Leonie Enders [Allemagne] ; Rachel Saunders-Pullman [États-Unis] ; Susan B. Bressman [États-Unis] ; Alexander Münchau [Allemagne] ; Christine Klein [Allemagne] ; Johann Hagenah [Allemagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2011-02-15.
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Abstract
Background: Musician's dystonia (MD) is traditionally considered a sporadic and task‐specific movement disorder. Methods: The phenotypic spectrum of the disorder was studied in 116 patients suffering from MD including videotaping. Results: Based on the movement disorders observed, we categorized our patients into two different groups: (i) 65 patients with isolated MD, that is only present when playing the instrument and (ii) 51 patients with MD and one or more additional features of primary dystonia independent of MD (complex MD). Patients with a positive family history of movement disorders had an increased risk to develop complex MD [odds ratio = 4.80; 95% confidence interval: 1.94–11.92; P = 0.001]. Discussion: In previous studies, we recently identified 22 relatives with different types of movement disorders in the families of 28 MD patients. Taken together, our results further support a genetic contribution to MD with a broad individual and familial phenotypic spectrum consisting of MD, other dystonias and even other, non‐dystonic movement disorders. © 2010 Movement Disorder Society
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DOI: 10.1002/mds.23526
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Lübeck</wicri:regionArea></affiliation><affiliation wicri:level="1"><mods:affiliation>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama, Hanover, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama, Hanover</wicri:regionArea></affiliation></author><author><name sortKey="Jabusch, Hans Hristian" sort="Jabusch, Hans Hristian" uniqKey="Jabusch H" first="Hans-Christian" last="Jabusch">Hans-Christian Jabusch</name><affiliation wicri:level="1"><mods:affiliation>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama, Hanover, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama, Hanover</wicri:regionArea></affiliation><affiliation wicri:level="1"><mods:affiliation>Institute of Musicians' Medicine, Dresden University of Music “Carl Maria von Weber”, Dresden, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Institute of Musicians' Medicine, Dresden University of Music “Carl Maria von Weber”, Dresden</wicri:regionArea></affiliation></author><author><name sortKey="Altenmuller, Eckart" sort="Altenmuller, Eckart" uniqKey="Altenmuller E" first="Eckart" last="Altenmüller">Eckart Altenmüller</name><affiliation wicri:level="1"><mods:affiliation>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama, Hanover, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama, Hanover</wicri:regionArea></affiliation></author><author><name sortKey="Enders, Leonie" sort="Enders, Leonie" uniqKey="Enders L" first="Leonie" last="Enders">Leonie Enders</name><affiliation wicri:level="1"><mods:affiliation>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama, Hanover, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama, Hanover</wicri:regionArea></affiliation></author><author><name sortKey="Saunders Ullman, Rachel" sort="Saunders Ullman, Rachel" uniqKey="Saunders Ullman R" first="Rachel" last="Saunders-Pullman">Rachel Saunders-Pullman</name><affiliation wicri:level="1"><mods:affiliation>Department of Neurology, Albert Einstein College of Medicine, Bronx, New York, USA</mods:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Neurology, Albert Einstein College of Medicine, Bronx, New York</wicri:regionArea></affiliation><affiliation wicri:level="1"><mods:affiliation>Department of Neurology, Beth Israel Medical Center, New York, New York, USA</mods:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Neurology, Beth Israel Medical Center, New York, New York</wicri:regionArea></affiliation></author><author><name sortKey="Bressman, Susan B" sort="Bressman, Susan B" uniqKey="Bressman S" first="Susan B." last="Bressman">Susan B. Bressman</name><affiliation wicri:level="1"><mods:affiliation>Department of Neurology, Albert Einstein College of Medicine, Bronx, New York, USA</mods:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Neurology, Albert Einstein College of Medicine, Bronx, New York</wicri:regionArea></affiliation><affiliation wicri:level="1"><mods:affiliation>Department of Neurology, Beth Israel Medical Center, New York, New York, USA</mods:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Neurology, Beth Israel Medical Center, New York, New York</wicri:regionArea></affiliation></author><author><name sortKey="Munchau, Alexander" sort="Munchau, Alexander" uniqKey="Munchau A" first="Alexander" last="Münchau">Alexander Münchau</name><affiliation wicri:level="1"><mods:affiliation>Department of Neurology, University Medical Center Hamburg‐Eppendorf, Hamburg, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Department of Neurology, University Medical Center Hamburg‐Eppendorf, Hamburg</wicri:regionArea></affiliation></author><author><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name><affiliation wicri:level="1"><mods:affiliation>Section of Clinical and Molecular Neurogenetics, University of Lüebeck, Lübeck, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Section of Clinical and Molecular Neurogenetics, University of Lüebeck, Lübeck</wicri:regionArea></affiliation><affiliation wicri:level="1"><mods:affiliation>Department of Neurology, University of Lüebeck, Lübeck, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Department of Neurology, University of Lüebeck, Lübeck</wicri:regionArea></affiliation></author><author><name sortKey="Hagenah, Johann" sort="Hagenah, Johann" uniqKey="Hagenah J" first="Johann" last="Hagenah">Johann Hagenah</name><affiliation wicri:level="1"><mods:affiliation>Section of Clinical and Molecular Neurogenetics, University of Lüebeck, Lübeck, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Section of Clinical and Molecular Neurogenetics, University of Lüebeck, Lübeck</wicri:regionArea></affiliation><affiliation wicri:level="1"><mods:affiliation>Department of Neurology, University of Lüebeck, Lübeck, Germany</mods:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Department of Neurology, University of Lüebeck, Lübeck</wicri:regionArea></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</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="2011-02-15">2011-02-15</date><biblScope unit="vol">26</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="546">546</biblScope><biblScope unit="page" to="549">549</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">79FFA8F00268F7B66D1AD700A89BE9F6371CD6E7</idno><idno type="DOI">10.1002/mds.23526</idno><idno type="ArticleID">MDS23526</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>focal task‐specific dystonia</term><term>genetics</term><term>movement disorders</term><term>musician's dystonia</term><term>writer's cramp</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background: Musician's dystonia (MD) is traditionally considered a sporadic and task‐specific movement disorder. Methods: The phenotypic spectrum of the disorder was studied in 116 patients suffering from MD including videotaping. Results: Based on the movement disorders observed, we categorized our patients into two different groups: (i) 65 patients with isolated MD, that is only present when playing the instrument and (ii) 51 patients with MD and one or more additional features of primary dystonia independent of MD (complex MD). Patients with a positive family history of movement disorders had an increased risk to develop complex MD [odds ratio = 4.80; 95% confidence interval: 1.94–11.92; P = 0.001]. Discussion: In previous studies, we recently identified 22 relatives with different types of movement disorders in the families of 28 MD patients. Taken together, our results further support a genetic contribution to MD with a broad individual and familial phenotypic spectrum consisting of MD, other dystonias and even other, non‐dystonic movement disorders. © 2010 Movement Disorder Society</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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