Moyamoya‐induced paroxysmal dyskinesia
Identifieur interne : 001397 ( Main/Exploration ); précédent : 001396; suivant : 001398Moyamoya‐induced paroxysmal dyskinesia
Auteurs : Pedro Gonzalez [États-Unis] ; Zakaria Ammache [États-Unis] ; Patricia Davis [États-Unis] ; Robert Rodnitzky [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2003-09.
English descriptors
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Abstract
Moyamoya disease (MMD) is an uncommon intracranial vasculopathy that typically presents with ischemic or hemorrhagic stroke. Persistent choreoathetosis has been identified as a rare early manifestation of MMD. We present 2 patients with paroxysmal dyskinesia as the initial symptom of MMD, one resembling paroxysmal kinesigenic dyskinesia (PKD) and the other paroxysmal non‐kinesigenic dyskinesia (PNKD). We also review the cases of moyamoya‐induced chorea reported previously, none of which resembled PKD or PNKD. We hypothesize that both hormonal and ischemic factors may be implicated in the pathogenesis of these abnormal involuntary movements. These cases suggest that MMD should be included in the differential diagnosis of PKD and PNKD. © 2003 Movement Disorder Society
Url:
DOI: 10.1002/mds.10483
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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="2003-09">2003-09</date><biblScope unit="volume">18</biblScope><biblScope unit="issue">9</biblScope><biblScope unit="page" from="1051">1051</biblScope><biblScope unit="page" to="1056">1056</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">995D2CE1991C52E056A1774DE46AD2FC687C5911</idno><idno type="DOI">10.1002/mds.10483</idno><idno type="ArticleID">MDS10483</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>moyamoya</term><term>paroxysmal dyskinesia</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Moyamoya disease (MMD) is an uncommon intracranial vasculopathy that typically presents with ischemic or hemorrhagic stroke. Persistent choreoathetosis has been identified as a rare early manifestation of MMD. We present 2 patients with paroxysmal dyskinesia as the initial symptom of MMD, one resembling paroxysmal kinesigenic dyskinesia (PKD) and the other paroxysmal non‐kinesigenic dyskinesia (PNKD). We also review the cases of moyamoya‐induced chorea reported previously, none of which resembled PKD or PNKD. We hypothesize that both hormonal and ischemic factors may be implicated in the pathogenesis of these abnormal involuntary movements. These cases suggest that MMD should be included in the differential diagnosis of PKD and PNKD. © 2003 Movement Disorder Society</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>Iowa</li></region></list><tree><country name="États-Unis"><region name="Iowa"><name sortKey="Gonzalez Legre, Pedro" sort="Gonzalez Legre, Pedro" uniqKey="Gonzalez Legre P" first="Pedro" last="Gonzalez">Pedro Gonzalez</name></region><name sortKey="Ammache, Zakaria" sort="Ammache, Zakaria" uniqKey="Ammache Z" first="Zakaria" last="Ammache">Zakaria Ammache</name><name sortKey="Davis, Patricia H" sort="Davis, Patricia H" uniqKey="Davis P" first="Patricia" last="Davis">Patricia Davis</name><name sortKey="Rodnitzky, Robert L" sort="Rodnitzky, Robert L" uniqKey="Rodnitzky R" first="Robert" last="Rodnitzky">Robert Rodnitzky</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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