Phenotypic spectrum of musician's dystonia: A task‐specific disorder?
Identifieur interne : 001466 ( Main/Exploration ); précédent : 001465; suivant : 001467Phenotypic spectrum of musician's dystonia: A task‐specific disorder?
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.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- MESH :
- physiopathology : Dystonic Disorders.
- Adolescent, Adult, Aged, Female, Humans, Male, Middle Aged, Music, Phenotype, Young Adult.
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
Url:
DOI: 10.1002/mds.23526
Affiliations:
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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>Adolescent</term><term>Adult</term><term>Aged</term><term>Dystonia</term><term>Dystonic Disorders (physiopathology)</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Music</term><term>Musician</term><term>Nervous system diseases</term><term>Phenotype</term><term>Writer cramp</term><term>Young Adult</term><term>focal task‐specific dystonia</term><term>genetics</term><term>movement disorders</term><term>musician's dystonia</term><term>writer's cramp</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Dystonic Disorders</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Aged</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Music</term><term>Phenotype</term><term>Young Adult</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Crampe écrivain</term><term>Dystonie</term><term>Musicien</term><term>Pathologie du système nerveux</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><affiliations><list><country><li>Allemagne</li><li>États-Unis</li></country><region><li>District de Dresde</li><li>Hambourg</li><li>Saxe (Land)</li><li>État de New York</li></region><settlement><li>Dresde</li><li>Hambourg</li></settlement></list><tree><country name="Allemagne"><noRegion><name sortKey="Schmidt, Alexander" sort="Schmidt, Alexander" uniqKey="Schmidt A" first="Alexander" last="Schmidt">Alexander Schmidt</name></noRegion><name sortKey="Altenmuller, Eckart" sort="Altenmuller, Eckart" uniqKey="Altenmuller E" first="Eckart" last="Altenmüller">Eckart Altenmüller</name><name sortKey="Enders, Leonie" sort="Enders, Leonie" uniqKey="Enders L" first="Leonie" last="Enders">Leonie Enders</name><name sortKey="Hagenah, Johann" sort="Hagenah, Johann" uniqKey="Hagenah J" first="Johann" last="Hagenah">Johann Hagenah</name><name sortKey="Hagenah, Johann" sort="Hagenah, Johann" uniqKey="Hagenah J" first="Johann" last="Hagenah">Johann Hagenah</name><name sortKey="Jabusch, Hans Hristian" sort="Jabusch, Hans Hristian" uniqKey="Jabusch H" first="Hans-Christian" last="Jabusch">Hans-Christian Jabusch</name><name sortKey="Jabusch, Hans Hristian" sort="Jabusch, Hans Hristian" uniqKey="Jabusch H" first="Hans-Christian" last="Jabusch">Hans-Christian Jabusch</name><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name><name sortKey="Munchau, Alexander" sort="Munchau, Alexander" uniqKey="Munchau A" first="Alexander" last="Münchau">Alexander Münchau</name><name sortKey="Schmidt, Alexander" sort="Schmidt, Alexander" uniqKey="Schmidt A" first="Alexander" last="Schmidt">Alexander Schmidt</name><name sortKey="Schmidt, Alexander" sort="Schmidt, Alexander" uniqKey="Schmidt A" first="Alexander" last="Schmidt">Alexander Schmidt</name></country><country name="États-Unis"><region name="État de New York"><name sortKey="Saunders Ullman, Rachel" sort="Saunders Ullman, Rachel" uniqKey="Saunders Ullman R" first="Rachel" last="Saunders-Pullman">Rachel Saunders-Pullman</name></region><name sortKey="Bressman, Susan B" sort="Bressman, Susan B" uniqKey="Bressman S" first="Susan B." last="Bressman">Susan B. Bressman</name><name sortKey="Bressman, Susan B" sort="Bressman, Susan B" uniqKey="Bressman S" first="Susan B." last="Bressman">Susan B. Bressman</name><name sortKey="Saunders Ullman, Rachel" sort="Saunders Ullman, Rachel" uniqKey="Saunders Ullman R" first="Rachel" last="Saunders-Pullman">Rachel Saunders-Pullman</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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