MovDisordV3, PubMed, Corpus, bibRecord, 005063

Hereditary myoclonus and chorea: the spectrum of hereditary nonprogressive hyperkinetic movement disorders.

Identifieur interne : 005063 ( PubMed/Corpus ); précédent : 005062; suivant : 005064

Hereditary myoclonus and chorea: the spectrum of hereditary nonprogressive hyperkinetic movement disorders.

Auteurs : R. Kurlan ; J. Behr ; I. Shoulson

Source :

Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1987.

RBID : pubmed:3504555

English descriptors

KwdEn :
- Adult, Chorea (genetics), Dystonia (genetics), Female, Follow-Up Studies, Gait, Humans, Male, Middle Aged, Myoclonus (genetics).
MESH :
- genetics : Chorea, Dystonia, Myoclonus.
- Adult, Female, Follow-Up Studies, Gait, Humans, Male, Middle Aged.

Abstract

We report three members of a single family who developed a newly described combination of myoclonus and chorea in association with mild ataxia. The occurrence of this and related syndromes suggests that inherited, slowly progressive myoclonus, chorea, and dystonia, alone or in combination, should be viewed as a spectrum of hyperkinetic involuntary movements, and that each motor component may represent variable expression of the same genetic defect.

DOI: 10.1002/mds.870020407
PubMed: 3504555

Links to Exploration step

pubmed:3504555

Le document en format XML

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<author><name sortKey="Kurlan, R" sort="Kurlan, R" uniqKey="Kurlan R" first="R" last="Kurlan">R. Kurlan</name>
<affiliation><nlm:affiliation>Department of Neurology, University of Rochester School of Medicine, New York 14642.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Behr, J" sort="Behr, J" uniqKey="Behr J" first="J" last="Behr">J. Behr</name>
</author>
<author><name sortKey="Shoulson, I" sort="Shoulson, I" uniqKey="Shoulson I" first="I" last="Shoulson">I. Shoulson</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Hereditary myoclonus and chorea: the spectrum of hereditary nonprogressive hyperkinetic movement disorders.</title>
<author><name sortKey="Kurlan, R" sort="Kurlan, R" uniqKey="Kurlan R" first="R" last="Kurlan">R. Kurlan</name>
<affiliation><nlm:affiliation>Department of Neurology, University of Rochester School of Medicine, New York 14642.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Behr, J" sort="Behr, J" uniqKey="Behr J" first="J" last="Behr">J. Behr</name>
</author>
<author><name sortKey="Shoulson, I" sort="Shoulson, I" uniqKey="Shoulson I" first="I" last="Shoulson">I. Shoulson</name>
</author>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="1987" type="published">1987</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Chorea (genetics)</term>
<term>Dystonia (genetics)</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Gait</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Myoclonus (genetics)</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chorea</term>
<term>Dystonia</term>
<term>Myoclonus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Gait</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
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<front><div type="abstract" xml:lang="en">We report three members of a single family who developed a newly described combination of myoclonus and chorea in association with mild ataxia. The occurrence of this and related syndromes suggests that inherited, slowly progressive myoclonus, chorea, and dystonia, alone or in combination, should be viewed as a spectrum of hyperkinetic involuntary movements, and that each motor component may represent variable expression of the same genetic defect.</div>
</front>
</TEI>
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<DateCreated><Year>1989</Year>
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<DateCompleted><Year>1989</Year>
<Month>01</Month>
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<DateRevised><Year>2004</Year>
<Month>11</Month>
<Day>17</Day>
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<Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print"><Volume>2</Volume>
<Issue>4</Issue>
<PubDate><Year>1987</Year>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>Hereditary myoclonus and chorea: the spectrum of hereditary nonprogressive hyperkinetic movement disorders.</ArticleTitle>
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<Abstract><AbstractText>We report three members of a single family who developed a newly described combination of myoclonus and chorea in association with mild ataxia. The occurrence of this and related syndromes suggests that inherited, slowly progressive myoclonus, chorea, and dystonia, alone or in combination, should be viewed as a spectrum of hyperkinetic involuntary movements, and that each motor component may represent variable expression of the same genetic defect.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Kurlan</LastName>
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<AffiliationInfo><Affiliation>Department of Neurology, University of Rochester School of Medicine, New York 14642.</Affiliation>
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<Author ValidYN="Y"><LastName>Behr</LastName>
<ForeName>J</ForeName>
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<Author ValidYN="Y"><LastName>Shoulson</LastName>
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<Initials>I</Initials>
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<Language>eng</Language>
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<MedlineJournalInfo><Country>UNITED STATES</Country>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004421">Dystonia</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005500">Follow-Up Studies</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005684">Gait</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009207">Myoclonus</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
</MeshHeadingList>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Hereditary myoclonus and chorea: the spectrum of hereditary nonprogressive hyperkinetic movement disorders.

Hereditary myoclonus and chorea: the spectrum of hereditary nonprogressive hyperkinetic movement disorders.

Source :

English descriptors

Abstract

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki