Markedly asymmetrical parkinsonism as a leading feature of adult-onset Huntington's disease.
Identifieur interne : 000E86 ( Ncbi/Merge ); précédent : 000E85; suivant : 000E87Markedly asymmetrical parkinsonism as a leading feature of adult-onset Huntington's disease.
Auteurs : Shih-Ching Wang [Taïwan] ; Guey-Jen Lee-Chen ; Cheng-Kung Wang ; Chiung-Mei Chen ; Lok-Ming Tang ; Yih-Ru WuSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2004.
English descriptors
- KwdEn :
- Adult, Alleles, Antiparkinson Agents (therapeutic use), Carbidopa (therapeutic use), Cognition Disorders (diagnosis), Cognition Disorders (etiology), Diagnosis, Differential, Drug Combinations, Humans, Huntington Disease (complications), Huntington Disease (diagnosis), Huntington Disease (genetics), Levodopa (therapeutic use), Male, Neuropsychological Tests, Parkinsonian Disorders (diagnosis), Parkinsonian Disorders (drug therapy), Pedigree, Severity of Illness Index.
- MESH :
- chemical , therapeutic use : Antiparkinson Agents, Carbidopa, Levodopa.
- complications : Huntington Disease.
- diagnosis : Cognition Disorders, Huntington Disease, Parkinsonian Disorders.
- drug therapy : Parkinsonian Disorders.
- etiology : Cognition Disorders.
- genetics : Huntington Disease.
- Adult, Alleles, Diagnosis, Differential, Drug Combinations, Humans, Male, Neuropsychological Tests, Pedigree, Severity of Illness Index.
Abstract
We report on a 28-year-old man who presented with right hand tremor, bradykinesia, and rigidity of his right side extremities. Our case report emphasizes that markedly asymmetrical parkinsonism can be an initial presentation of adult-onset Huntington's disease (HD), and different clinical presentations can be observed in members of an individual HD family with the same CAG repeat length.
DOI: 10.1002/mds.20093
PubMed: 15254954
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- to stream PubMed, to step Corpus: 003398
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pubmed:15254954Le document en format XML
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<author><name sortKey="Wang, Shih Ching" sort="Wang, Shih Ching" uniqKey="Wang S" first="Shih-Ching" last="Wang">Shih-Ching Wang</name>
<affiliation wicri:level="1"><nlm:affiliation>Second Department of Neurology, Chang Gung Memorial Hospital, LinKou Medical Center, Taipei, Taiwan.</nlm:affiliation>
<country xml:lang="fr">Taïwan</country>
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<author><name sortKey="Lee Chen, Guey Jen" sort="Lee Chen, Guey Jen" uniqKey="Lee Chen G" first="Guey-Jen" last="Lee-Chen">Guey-Jen Lee-Chen</name>
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<author><name sortKey="Wang, Cheng Kung" sort="Wang, Cheng Kung" uniqKey="Wang C" first="Cheng-Kung" last="Wang">Cheng-Kung Wang</name>
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<author><name sortKey="Chen, Chiung Mei" sort="Chen, Chiung Mei" uniqKey="Chen C" first="Chiung-Mei" last="Chen">Chiung-Mei Chen</name>
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<author><name sortKey="Tang, Lok Ming" sort="Tang, Lok Ming" uniqKey="Tang L" first="Lok-Ming" last="Tang">Lok-Ming Tang</name>
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<author><name sortKey="Wu, Yih Ru" sort="Wu, Yih Ru" uniqKey="Wu Y" first="Yih-Ru" last="Wu">Yih-Ru Wu</name>
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<term>Cognition Disorders (diagnosis)</term>
<term>Cognition Disorders (etiology)</term>
<term>Diagnosis, Differential</term>
<term>Drug Combinations</term>
<term>Humans</term>
<term>Huntington Disease (complications)</term>
<term>Huntington Disease (diagnosis)</term>
<term>Huntington Disease (genetics)</term>
<term>Levodopa (therapeutic use)</term>
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<term>Neuropsychological Tests</term>
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<front><div type="abstract" xml:lang="en">We report on a 28-year-old man who presented with right hand tremor, bradykinesia, and rigidity of his right side extremities. Our case report emphasizes that markedly asymmetrical parkinsonism can be an initial presentation of adult-onset Huntington's disease (HD), and different clinical presentations can be observed in members of an individual HD family with the same CAG repeat length.</div>
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<Abstract><AbstractText>We report on a 28-year-old man who presented with right hand tremor, bradykinesia, and rigidity of his right side extremities. Our case report emphasizes that markedly asymmetrical parkinsonism can be an initial presentation of adult-onset Huntington's disease (HD), and different clinical presentations can be observed in members of an individual HD family with the same CAG repeat length.</AbstractText>
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