MovDisordV3, PascalFrancis, Corpus, bibRecord, 000660

Phenotypic Spectrum of Musician's Dystonia: A Task-Specific Disorder?

Identifieur interne : 000660 ( PascalFrancis/Corpus ); précédent : 000659; suivant : 000661

Phenotypic Spectrum of Musician's Dystonia: A Task-Specific Disorder?

Auteurs : Alexander Schmidt ; Hans-Christian Jabusch ; Eckart Altenmüller ; Leonie Enders ; Rachel Saunders-Pullman ; Susan B. Bressman ; Alexander Munchau ; Christine Klein ; Johann Hagenah

Source :

Movement disorders [ 0885-3185 ] ; 2011.

RBID : Pascal:11-0211322

Descripteurs français

Pascal (Inist)
- Dystonie, Crampe écrivain, Pathologie du système nerveux, Musicien.

English descriptors

KwdEn :
- Dystonia, Musician, Nervous system diseases, Writer cramp.

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.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

A01	`01`	`1`		`@0 0885-3185`
A03		`1`		`@0 Mov. disord.`
A05				`@2 26`
A06				`@2 3`
A08	`01`	`1`	`ENG`	`@1 Phenotypic Spectrum of Musician's Dystonia: A Task-Specific Disorder?`
A11	`01`	`1`		`@1 SCHMIDT (Alexander)`
A11	`02`	`1`		`@1 JABUSCH (Hans-Christian)`
A11	`03`	`1`		`@1 ALTENMÜLLER (Eckart)`
A11	`04`	`1`		`@1 ENDERS (Leonie)`
A11	`05`	`1`		`@1 SAUNDERS-PULLMAN (Rachel)`
A11	`06`	`1`		`@1 BRESSMAN (Susan B.)`
A11	`07`	`1`		`@1 MUNCHAU (Alexander)`
A11	`08`	`1`		`@1 KLEIN (Christine)`
A11	`09`	`1`		`@1 HAGENAH (Johann)`
A14	`01`			`@1 Section of Clinical and Molecular Neurogenetics, University of Lüebeck @2 Lübeck @3 DEU @Z 1 aut. @Z 8 aut. @Z 9 aut.`
A14	`02`			`@1 Department of Neurology, University of Lüebeck @2 Lübeck @3 DEU @Z 1 aut. @Z 8 aut. @Z 9 aut.`
A14	`03`			`@1 Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama @2 Hanover @3 DEU @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut.`
A14	`04`			`@1 Institute of Musicians' Medicine, Dresden University of Music "Carl Maria von Weber" @2 Dresden @3 DEU @Z 2 aut.`
A14	`05`			`@1 Department of Neurology, Albert Einstein College of Medicine @2 Bronx, New York @3 USA @Z 5 aut. @Z 6 aut.`
A14	`06`			`@1 Department of Neurology, Beth Israel Medical Center, New York @2 New York @3 USA @Z 5 aut. @Z 6 aut.`
A14	`07`			`@1 Department of Neurology, University Medical Center Hamburg-Eppendorf @2 Hamburg @3 DEU @Z 7 aut.`
A20				`@1 546-549`
A21				`@1 2011`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000190875360270`
A44				`@0 0000 @1 © 2011 INIST-CNRS. All rights reserved.`
A45				`@0 8 ref.`
A47	`01`	`1`		`@0 11-0211322`
A60				`@1 P @3 CC`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C01	`01`		`ENG`	@0 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.
C02	`01`	`X`		`@0 002B17`
C02	`02`	`X`		`@0 002B17H`
C03	`01`	`X`	`FRE`	`@0 Dystonie @5 01`
C03	`01`	`X`	`ENG`	`@0 Dystonia @5 01`
C03	`01`	`X`	`SPA`	`@0 Distonía @5 01`
C03	`02`	`X`	`FRE`	`@0 Crampe écrivain @5 02`
C03	`02`	`X`	`ENG`	`@0 Writer cramp @5 02`
C03	`02`	`X`	`SPA`	`@0 Calambre escribano @5 02`
C03	`03`	`X`	`FRE`	`@0 Pathologie du système nerveux @5 03`
C03	`03`	`X`	`ENG`	`@0 Nervous system diseases @5 03`
C03	`03`	`X`	`SPA`	`@0 Sistema nervioso patología @5 03`
C03	`04`	`X`	`FRE`	`@0 Musicien @5 09`
C03	`04`	`X`	`ENG`	`@0 Musician @5 09`
C03	`04`	`X`	`SPA`	`@0 Músico @5 09`
C07	`01`	`X`	`FRE`	`@0 Syndrome extrapyramidal @5 37`
C07	`01`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 37`
C07	`01`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 37`
C07	`02`	`X`	`FRE`	`@0 Mouvement involontaire @5 38`
C07	`02`	`X`	`ENG`	`@0 Involuntary movement @5 38`
C07	`02`	`X`	`SPA`	`@0 Movimiento involuntario @5 38`
C07	`03`	`X`	`FRE`	`@0 Pathologie du muscle strié @5 39`
C07	`03`	`X`	`ENG`	`@0 Striated muscle disease @5 39`
C07	`03`	`X`	`SPA`	`@0 Músculo estriado patología @5 39`
C07	`04`	`X`	`FRE`	`@0 Trouble neurologique @5 41`
C07	`04`	`X`	`ENG`	`@0 Neurological disorder @5 41`
C07	`04`	`X`	`SPA`	`@0 Trastorno neurológico @5 41`
C07	`05`	`X`	`FRE`	`@0 Pathologie de l'encéphale @5 42`
C07	`05`	`X`	`ENG`	`@0 Cerebral disorder @5 42`
C07	`05`	`X`	`SPA`	`@0 Encéfalo patología @5 42`
C07	`06`	`X`	`FRE`	`@0 Pathologie du système nerveux central @5 43`
C07	`06`	`X`	`ENG`	`@0 Central nervous system disease @5 43`
C07	`06`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 43`
N21				`@1 143`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

Format Inist (serveur)

NO :	PASCAL 11-0211322 INIST
ET :	Phenotypic Spectrum of Musician's Dystonia: A Task-Specific Disorder?
AU :	SCHMIDT (Alexander); JABUSCH (Hans-Christian); ALTENMÜLLER (Eckart); ENDERS (Leonie); SAUNDERS-PULLMAN (Rachel); BRESSMAN (Susan B.); MUNCHAU (Alexander); KLEIN (Christine); HAGENAH (Johann)
AF :	Section of Clinical and Molecular Neurogenetics, University of Lüebeck/Lübeck/Allemagne (1 aut., 8 aut., 9 aut.); Department of Neurology, University of Lüebeck/Lübeck/Allemagne (1 aut., 8 aut., 9 aut.); Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama/Hanover/Allemagne (1 aut., 2 aut., 3 aut., 4 aut.); Institute of Musicians' Medicine, Dresden University of Music "Carl Maria von Weber"/Dresden/Allemagne (2 aut.); Department of Neurology, Albert Einstein College of Medicine/Bronx, New York/Etats-Unis (5 aut., 6 aut.); Department of Neurology, Beth Israel Medical Center, New York/New York/Etats-Unis (5 aut., 6 aut.); Department of Neurology, University Medical Center Hamburg-Eppendorf/Hamburg/Allemagne (7 aut.)
DT :	Publication en série; Courte communication, note brève; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2011; Vol. 26; No. 3; Pp. 546-549; Bibl. 8 ref.
LA :	Anglais
EA :	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.
CC :	002B17; 002B17H
FD :	Dystonie; Crampe écrivain; Pathologie du système nerveux; Musicien
FG :	Syndrome extrapyramidal; Mouvement involontaire; Pathologie du muscle strié; Trouble neurologique; Pathologie de l'encéphale; Pathologie du système nerveux central
ED :	Dystonia; Writer cramp; Nervous system diseases; Musician
EG :	Extrapyramidal syndrome; Involuntary movement; Striated muscle disease; Neurological disorder; Cerebral disorder; Central nervous system disease
SD :	Distonía; Calambre escribano; Sistema nervioso patología; Músico
LO :	INIST-20953.354000190875360270
ID :	11-0211322

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Pascal:11-0211322

Le document en format XML

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<author><name sortKey="Munchau, Alexander" sort="Munchau, Alexander" uniqKey="Munchau A" first="Alexander" last="Munchau">Alexander Munchau</name>
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<author><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name>
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<author><name sortKey="Hagenah, Johann" sort="Hagenah, Johann" uniqKey="Hagenah J" first="Johann" last="Hagenah">Johann Hagenah</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Phenotypic Spectrum of Musician's Dystonia: A Task-Specific Disorder?</title>
<author><name sortKey="Schmidt, Alexander" sort="Schmidt, Alexander" uniqKey="Schmidt A" first="Alexander" last="Schmidt">Alexander Schmidt</name>
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<affiliation><inist:fA14 i1="03"><s1>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama</s1>
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<author><name sortKey="Jabusch, Hans Christian" sort="Jabusch, Hans Christian" uniqKey="Jabusch H" first="Hans-Christian" last="Jabusch">Hans-Christian Jabusch</name>
<affiliation><inist:fA14 i1="03"><s1>Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama</s1>
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<affiliation><inist:fA14 i1="04"><s1>Institute of Musicians' Medicine, Dresden University of Music "Carl Maria von Weber"</s1>
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<author><name sortKey="Altenmuller, Eckart" sort="Altenmuller, Eckart" uniqKey="Altenmuller E" first="Eckart" last="Altenmüller">Eckart Altenmüller</name>
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<author><name sortKey="Enders, Leonie" sort="Enders, Leonie" uniqKey="Enders L" first="Leonie" last="Enders">Leonie Enders</name>
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<author><name sortKey="Saunders Pullman, Rachel" sort="Saunders Pullman, Rachel" uniqKey="Saunders Pullman R" first="Rachel" last="Saunders-Pullman">Rachel Saunders-Pullman</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Neurology, Albert Einstein College of Medicine</s1>
<s2>Bronx, New York</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
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</inist:fA14>
</affiliation>
<affiliation><inist:fA14 i1="06"><s1>Department of Neurology, Beth Israel Medical Center, New York</s1>
<s2>New York</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
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</author>
<author><name sortKey="Bressman, Susan B" sort="Bressman, Susan B" uniqKey="Bressman S" first="Susan B." last="Bressman">Susan B. Bressman</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Neurology, Albert Einstein College of Medicine</s1>
<s2>Bronx, New York</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation><inist:fA14 i1="06"><s1>Department of Neurology, Beth Israel Medical Center, New York</s1>
<s2>New York</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Munchau, Alexander" sort="Munchau, Alexander" uniqKey="Munchau A" first="Alexander" last="Munchau">Alexander Munchau</name>
<affiliation><inist:fA14 i1="07"><s1>Department of Neurology, University Medical Center Hamburg-Eppendorf</s1>
<s2>Hamburg</s2>
<s3>DEU</s3>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name>
<affiliation><inist:fA14 i1="01"><s1>Section of Clinical and Molecular Neurogenetics, University of Lüebeck</s1>
<s2>Lübeck</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation><inist:fA14 i1="02"><s1>Department of Neurology, University of Lüebeck</s1>
<s2>Lübeck</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>8 aut.</sZ>
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</author>
<author><name sortKey="Hagenah, Johann" sort="Hagenah, Johann" uniqKey="Hagenah J" first="Johann" last="Hagenah">Johann Hagenah</name>
<affiliation><inist:fA14 i1="01"><s1>Section of Clinical and Molecular Neurogenetics, University of Lüebeck</s1>
<s2>Lübeck</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
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<affiliation><inist:fA14 i1="02"><s1>Department of Neurology, University of Lüebeck</s1>
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<series><title level="j" type="main">Movement disorders</title>
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<imprint><date when="2011">2011</date>
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<term>Writer cramp</term>
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<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.</div>
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<sZ>6 aut.</sZ>
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<ET>Phenotypic Spectrum of Musician's Dystonia: A Task-Specific Disorder?</ET>
<AU>SCHMIDT (Alexander); JABUSCH (Hans-Christian); ALTENMÜLLER (Eckart); ENDERS (Leonie); SAUNDERS-PULLMAN (Rachel); BRESSMAN (Susan B.); MUNCHAU (Alexander); KLEIN (Christine); HAGENAH (Johann)</AU>
<AF>Section of Clinical and Molecular Neurogenetics, University of Lüebeck/Lübeck/Allemagne (1 aut., 8 aut., 9 aut.); Department of Neurology, University of Lüebeck/Lübeck/Allemagne (1 aut., 8 aut., 9 aut.); Institute of Music Physiology and Musicians' Medicine, Hanover University of Music and Drama/Hanover/Allemagne (1 aut., 2 aut., 3 aut., 4 aut.); Institute of Musicians' Medicine, Dresden University of Music "Carl Maria von Weber"/Dresden/Allemagne (2 aut.); Department of Neurology, Albert Einstein College of Medicine/Bronx, New York/Etats-Unis (5 aut., 6 aut.); Department of Neurology, Beth Israel Medical Center, New York/New York/Etats-Unis (5 aut., 6 aut.); Department of Neurology, University Medical Center Hamburg-Eppendorf/Hamburg/Allemagne (7 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
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<EA>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.</EA>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Phenotypic Spectrum of Musician's Dystonia: A Task-Specific Disorder?

Phenotypic Spectrum of Musician's Dystonia: A Task-Specific Disorder?

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