Feeding dystonia in McLeod Syndrome
Identifieur interne : 001660 ( Main/Exploration ); précédent : 001659; suivant : 001661Feeding dystonia in McLeod Syndrome
Auteurs : Andreas R. Gantenbein [Suisse] ; Nathalie Damon-Perrière [France] ; Jörg E. Bohlender [Suisse] ; Marie Chauveau [France] ; Chrystelle Latxague [France] ; Marcelo Miranda [Chili] ; Hans H. Jung [Suisse] ; François Tison [France]Source :
- Movement Disorders [ 0885-3185 ] ; 2011-09.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Aged, Dystonia, Dystonia (etiology), Feeding Behavior (physiology), Humans, MacLeod syndrome, Male, McLeod syndrome, Middle Aged, Nervous System Diseases (complications), Nervous System Diseases (genetics), Nervous system diseases, Neuroacanthocytosis (complications), Neuroacanthocytosis (genetics), Sex linked character, feeding dystonia, neuroacanthocytosis.
- MESH :
- complications : Nervous System Diseases, Neuroacanthocytosis.
- etiology : Dystonia.
- genetics : Nervous System Diseases, Neuroacanthocytosis.
- physiology : Feeding Behavior.
- Aged, Humans, Male, Middle Aged.
Abstract
Background:: The X‐linked McLeod syndrome belongs to the group of neuroacanthocytosis syndromes and has a Huntington‐disease–like phenotype with a choreatic movement disorder, cognitive alterations, and psychiatric symptoms. Another neuroacanthocytosis syndrome, the autosomal recessive chorea‐acanthocytosis, has a similar presentation, but distinct clinical features, believed to be characteristic, such as tongue protrusion dystonia, feeding dystonia, and rubber‐man–like appearance. Methods:: This work comprised a case series of 3 patients with McLeod syndrome. Results:: The 3 patients with McLeod syndrome developed severe feeding dystonia and tongue protrusion as well as rubber‐man–like appearance in 1 patient during the course of the disease. Conclusion:: These observations indicate that there is an extended phenotypic overlap between McLeod syndrome and chorea‐acanthocytosis. © 2011 Movement Disorder Society
Url:
DOI: 10.1002/mds.23843
Affiliations:
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Jung</name><affiliation wicri:level="3"><country xml:lang="fr">Suisse</country><wicri:regionArea>Department of Neurology, University Hospital Zürich, Zürich</wicri:regionArea><placeName><settlement type="city">Zurich</settlement><region nuts="3" type="region">Canton de Zurich</region></placeName></affiliation></author><author><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="François" last="Tison">François Tison</name><affiliation wicri:level="1"><country xml:lang="fr">France</country><wicri:regionArea>Department of Neurology, University Hospital Bordeaux, Bordeaux</wicri:regionArea><placeName><settlement type="city">Bordeaux</settlement></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. 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="2011-09">2011-09</date><biblScope unit="vol">26</biblScope><biblScope unit="issue">11</biblScope><biblScope unit="page" from="2123">2123</biblScope><biblScope unit="page" to="2126">2126</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">841D3B98EBAC3DC7F05DB4DC94613917A325A591</idno><idno type="DOI">10.1002/mds.23843</idno><idno type="ArticleID">MDS23843</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Dystonia</term><term>Dystonia (etiology)</term><term>Feeding Behavior (physiology)</term><term>Humans</term><term>MacLeod syndrome</term><term>Male</term><term>McLeod syndrome</term><term>Middle Aged</term><term>Nervous System Diseases (complications)</term><term>Nervous System Diseases (genetics)</term><term>Nervous system diseases</term><term>Neuroacanthocytosis (complications)</term><term>Neuroacanthocytosis (genetics)</term><term>Sex linked character</term><term>feeding dystonia</term><term>neuroacanthocytosis</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Nervous System Diseases</term><term>Neuroacanthocytosis</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Dystonia</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Nervous System Diseases</term><term>Neuroacanthocytosis</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Feeding Behavior</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Humans</term><term>Male</term><term>Middle Aged</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Caractère lié au sexe</term><term>Dystonie</term><term>Pathologie du système nerveux</term><term>Syndrome de MacLeod</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background:: The X‐linked McLeod syndrome belongs to the group of neuroacanthocytosis syndromes and has a Huntington‐disease–like phenotype with a choreatic movement disorder, cognitive alterations, and psychiatric symptoms. Another neuroacanthocytosis syndrome, the autosomal recessive chorea‐acanthocytosis, has a similar presentation, but distinct clinical features, believed to be characteristic, such as tongue protrusion dystonia, feeding dystonia, and rubber‐man–like appearance. Methods:: This work comprised a case series of 3 patients with McLeod syndrome. Results:: The 3 patients with McLeod syndrome developed severe feeding dystonia and tongue protrusion as well as rubber‐man–like appearance in 1 patient during the course of the disease. Conclusion:: These observations indicate that there is an extended phenotypic overlap between McLeod syndrome and chorea‐acanthocytosis. © 2011 Movement Disorder Society</div></front></TEI><affiliations><list><country><li>Chili</li><li>France</li><li>Suisse</li></country><region><li>Canton de Zurich</li></region><settlement><li>Bordeaux</li><li>Zurich</li></settlement></list><tree><country name="Suisse"><region name="Canton de Zurich"><name sortKey="Gantenbein, Andreas R" sort="Gantenbein, Andreas R" uniqKey="Gantenbein A" first="Andreas R." last="Gantenbein">Andreas R. Gantenbein</name></region><name sortKey="Bohlender, Jorg E" sort="Bohlender, Jorg E" uniqKey="Bohlender J" first="Jörg E." last="Bohlender">Jörg E. Bohlender</name><name sortKey="Jung, Hans H" sort="Jung, Hans H" uniqKey="Jung H" first="Hans H." last="Jung">Hans H. Jung</name></country><country name="France"><noRegion><name sortKey="Damon Erriere, Nathalie" sort="Damon Erriere, Nathalie" uniqKey="Damon Erriere N" first="Nathalie" last="Damon-Perrière">Nathalie Damon-Perrière</name></noRegion><name sortKey="Chauveau, Marie" sort="Chauveau, Marie" uniqKey="Chauveau M" first="Marie" last="Chauveau">Marie Chauveau</name><name sortKey="Latxague, Chrystelle" sort="Latxague, Chrystelle" uniqKey="Latxague C" first="Chrystelle" last="Latxague">Chrystelle Latxague</name><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="François" last="Tison">François Tison</name></country><country name="Chili"><noRegion><name sortKey="Miranda, Marcelo" sort="Miranda, Marcelo" uniqKey="Miranda M" first="Marcelo" last="Miranda">Marcelo Miranda</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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