X‐linked dystonia (“Lubag”) presenting predominantly with parkinsonism: A more benign phenotype?
Identifieur interne : 004236 ( Main/Exploration ); précédent : 004235; suivant : 004237X‐linked dystonia (“Lubag”) presenting predominantly with parkinsonism: A more benign phenotype?
Auteurs : Virgilio Gerald H. Evidente [États-Unis, Philippines] ; Katrina Gwinn-Hardy [États-Unis] ; John Hardy [États-Unis] ; Dena Hernandez [États-Unis] ; Andrew Singleton [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2002-01.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Adulte.
English descriptors
- KwdEn :
- Adult, Antiparkinson Agents (therapeutic use), Case study, Chromosome Aberrations, Diagnosis, Dystonia, Dystonic Disorders (complications), Dystonic Disorders (drug therapy), Dystonic Disorders (genetics), Evolution, Humans, Inaugural sign, Levodopa (therapeutic use), Male, Parkinsonian Disorders (complications), Parkinsonian Disorders (drug therapy), Parkinsonism, Phenotype, Sex linked character, X Chromosome (genetics), X-Chromosome.
- MESH :
- chemical , therapeutic use : Antiparkinson Agents, Levodopa.
- complications : Dystonic Disorders, Parkinsonian Disorders.
- drug therapy : Dystonic Disorders, Parkinsonian Disorders.
- genetics : Dystonic Disorders, X Chromosome.
- Adult, Chromosome Aberrations, Humans, Male, Phenotype.
Abstract
“Lubag,” or Filipino X‐linked dystonia, typically presents with either pure dystonia (that inexorably becomes generalized) or combined dystonia–parkinsonism. We report on three cases of Lubag presenting with isolated parkinsonism without dystonia or late‐onset dystonia and a slower course. © 2001 Movement Disorder Society.
Url:
DOI: 10.1002/mds.1263
Affiliations:
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Le document en format XML
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Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>John Wiley & Sons, Inc.</publisher><pubPlace>New York</pubPlace><date type="published" when="2002-01">2002-01</date><biblScope unit="vol">17</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="200">200</biblScope><biblScope unit="page" to="202">202</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">15661F5B0B47B2C8E63726E5FBC062AD8EB5C621</idno><idno type="DOI">10.1002/mds.1263</idno><idno type="ArticleID">MDS1263</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Antiparkinson Agents (therapeutic use)</term><term>Case study</term><term>Chromosome Aberrations</term><term>Diagnosis</term><term>Dystonia</term><term>Dystonic Disorders (complications)</term><term>Dystonic Disorders (drug therapy)</term><term>Dystonic Disorders (genetics)</term><term>Evolution</term><term>Humans</term><term>Inaugural sign</term><term>Levodopa (therapeutic use)</term><term>Male</term><term>Parkinsonian Disorders (complications)</term><term>Parkinsonian Disorders (drug therapy)</term><term>Parkinsonism</term><term>Phenotype</term><term>Sex linked character</term><term>X Chromosome (genetics)</term><term>X-Chromosome</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Antiparkinson Agents</term><term>Levodopa</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Dystonic Disorders</term><term>Parkinsonian Disorders</term></keywords><keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Dystonic Disorders</term><term>Parkinsonian Disorders</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Dystonic Disorders</term><term>X Chromosome</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Chromosome Aberrations</term><term>Humans</term><term>Male</term><term>Phenotype</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Adulte</term><term>Caractère lié au sexe</term><term>Chromosome X</term><term>Diagnostic</term><term>Dystonie</term><term>Etude cas</term><term>Evolution</term><term>Mâle</term><term>Parkinsonisme</term><term>Phénotype</term><term>Signe inaugural</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Adulte</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">“Lubag,” or Filipino X‐linked dystonia, typically presents with either pure dystonia (that inexorably becomes generalized) or combined dystonia–parkinsonism. We report on three cases of Lubag presenting with isolated parkinsonism without dystonia or late‐onset dystonia and a slower course. © 2001 Movement Disorder Society.</div></front></TEI><affiliations><list><country><li>Philippines</li><li>États-Unis</li></country><region><li>Arizona</li><li>Floride</li></region></list><tree><country name="États-Unis"><region name="Arizona"><name sortKey="Evidente, Virgilio Gerald H" sort="Evidente, Virgilio Gerald H" uniqKey="Evidente V" first="Virgilio Gerald H." last="Evidente">Virgilio Gerald H. Evidente</name></region><name sortKey="Gwinn Ardy, Katrina" sort="Gwinn Ardy, Katrina" uniqKey="Gwinn Ardy K" first="Katrina" last="Gwinn-Hardy">Katrina Gwinn-Hardy</name><name sortKey="Hardy, John" sort="Hardy, John" uniqKey="Hardy J" first="John" last="Hardy">John Hardy</name><name sortKey="Hernandez, Dena" sort="Hernandez, Dena" uniqKey="Hernandez D" first="Dena" last="Hernandez">Dena Hernandez</name><name sortKey="Singleton, Andrew" sort="Singleton, Andrew" uniqKey="Singleton A" first="Andrew" last="Singleton">Andrew Singleton</name></country><country name="Philippines"><noRegion><name sortKey="Evidente, Virgilio Gerald H" sort="Evidente, Virgilio Gerald H" uniqKey="Evidente V" first="Virgilio Gerald H." last="Evidente">Virgilio Gerald H. Evidente</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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