Isolated lingual/palatal dystonia.
Identifieur interne : 004E19 ( PubMed/Checkpoint ); précédent : 004E18; suivant : 004E20Isolated lingual/palatal dystonia.
Auteurs : D E Robertson-Hoffman ; M H Mark ; J I SageSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1991.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Dystonia, Tongue Diseases.
- physiopathology : Dystonia, Palatal Muscles, Tongue, Tongue Diseases.
- Female, Humans, Middle Aged, Neurologic Examination.
Abstract
We report a 45-year-old woman with a 3-year history of continuous dystonic movements of tongue and palate with intermittent episodes of noticeable worsening lasting 6 to 8 h. The movements began immediately after a viral illness. The only contributory history is that the patient received high doses of prochlorperazine 22 years earlier for hyperemesis gravidarum. The patient appears to have an unusual focal lower cranial dystonia. Proposed etiologies may be idiopathic or related to prior use of a phenothiazine with a viral trigger.
DOI: 10.1002/mds.870060217
PubMed: 2057012
Affiliations:
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pubmed:2057012Le document en format XML
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<author><name sortKey="Robertson Hoffman, D E" sort="Robertson Hoffman, D E" uniqKey="Robertson Hoffman D" first="D E" last="Robertson-Hoffman">D E Robertson-Hoffman</name>
<affiliation><nlm:affiliation>Department of Neurology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, New Brunswick 08903.</nlm:affiliation>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Isolated lingual/palatal dystonia.</title>
<author><name sortKey="Robertson Hoffman, D E" sort="Robertson Hoffman, D E" uniqKey="Robertson Hoffman D" first="D E" last="Robertson-Hoffman">D E Robertson-Hoffman</name>
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<author><name sortKey="Mark, M H" sort="Mark, M H" uniqKey="Mark M" first="M H" last="Mark">M H Mark</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Dystonia (diagnosis)</term>
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<term>Female</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
<term>Palatal Muscles (physiopathology)</term>
<term>Tongue (physiopathology)</term>
<term>Tongue Diseases (diagnosis)</term>
<term>Tongue Diseases (physiopathology)</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Dystonia</term>
<term>Tongue Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Dystonia</term>
<term>Palatal Muscles</term>
<term>Tongue</term>
<term>Tongue Diseases</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Female</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
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<front><div type="abstract" xml:lang="en">We report a 45-year-old woman with a 3-year history of continuous dystonic movements of tongue and palate with intermittent episodes of noticeable worsening lasting 6 to 8 h. The movements began immediately after a viral illness. The only contributory history is that the patient received high doses of prochlorperazine 22 years earlier for hyperemesis gravidarum. The patient appears to have an unusual focal lower cranial dystonia. Proposed etiologies may be idiopathic or related to prior use of a phenothiazine with a viral trigger.</div>
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<DateCreated><Year>1991</Year>
<Month>08</Month>
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<DateCompleted><Year>1991</Year>
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<JournalIssue CitedMedium="Print"><Volume>6</Volume>
<Issue>2</Issue>
<PubDate><Year>1991</Year>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Isolated lingual/palatal dystonia.</ArticleTitle>
<Pagination><MedlinePgn>177-9</MedlinePgn>
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<Abstract><AbstractText>We report a 45-year-old woman with a 3-year history of continuous dystonic movements of tongue and palate with intermittent episodes of noticeable worsening lasting 6 to 8 h. The movements began immediately after a viral illness. The only contributory history is that the patient received high doses of prochlorperazine 22 years earlier for hyperemesis gravidarum. The patient appears to have an unusual focal lower cranial dystonia. Proposed etiologies may be idiopathic or related to prior use of a phenothiazine with a viral trigger.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Robertson-Hoffman</LastName>
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<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D004421">Dystonia</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009460">Neurologic Examination</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010156">Palatal Muscles</DescriptorName>
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