Postural instability, frontotemporal dementia, and ophthalmoplegia: Clinicopathological case
Identifieur interne : 001463 ( Main/Curation ); précédent : 001462; suivant : 001464Postural instability, frontotemporal dementia, and ophthalmoplegia: Clinicopathological case
Auteurs : Francisco Cardoso [Brésil] ; John Hodges [Australie] ; Andrew H. Evans [Australie] ; Tamas Revesz [Royaume-Uni] ; David R. Williams [Royaume-Uni, Australie]Source :
- Movement Disorders [ 0885-3185 ] ; 2011-08-15.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Degeneration, Frontal Lobe (metabolism), Frontotemporal Dementia (complications), Frontotemporal Dementia (pathology), Frontotemporal dementia, Humans, Instability, Male, Middle Aged, Nervous system diseases, Ophthalmoplegia (complications), Ophthalmoplegia (pathology), Posture (physiology), Sensation Disorders (complications), Sensation Disorders (pathology), Supranuclear ophthalmoplegia, clinicopathological case, corticobasal degeneration, frontotemporal dementia, progressive supranuclear palsy, tau Proteins (metabolism).
- MESH :
- chemical , metabolism : tau Proteins.
- complications : Frontotemporal Dementia, Ophthalmoplegia, Sensation Disorders.
- metabolism : Frontal Lobe.
- pathology : Frontotemporal Dementia, Ophthalmoplegia, Sensation Disorders.
- physiology : Posture.
- Humans, Male, Middle Aged.
Abstract
A 56‐year‐old man presented with gait disturbance, personality change, and behavioral disturbances. He subsequently developed falls, postural instability, and axial rigidity. The cognitive problems progressed and he developed aphasia and later eye movement abnormalities. He died after 9 years of disease. Experts discuss the syndromal diagnosis and predict the underlying pathology. The pathological diagnosis is given and clinical learning points are considered. © 2011 Movement Disorder Society
Url:
DOI: 10.1002/mds.23359
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<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Postural instability, frontotemporal dementia, and ophthalmoplegia: Clinicopathological case</title>
<author><name sortKey="Cardoso, Francisco" sort="Cardoso, Francisco" uniqKey="Cardoso F" first="Francisco" last="Cardoso">Francisco Cardoso</name>
<affiliation wicri:level="3"><country xml:lang="fr">Brésil</country>
<wicri:regionArea>Movement Disorders Unit, Neurology Service, Federal University of Minas Gerais, Belo Horizonte</wicri:regionArea>
<placeName><settlement type="city">Belo Horizonte</settlement>
<region type="state">Minas Gerais</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Hodges, John" sort="Hodges, John" uniqKey="Hodges J" first="John" last="Hodges">John Hodges</name>
<affiliation wicri:level="3"><country xml:lang="fr">Australie</country>
<wicri:regionArea>Prince of Wales Medical Research Institute, University of New South Wales, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Evans, Andrew H" sort="Evans, Andrew H" uniqKey="Evans A" first="Andrew H." last="Evans">Andrew H. Evans</name>
<affiliation wicri:level="1"><country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Neurology, Royal Melbourne Hospital, Melbourne</wicri:regionArea>
<wicri:noRegion>Melbourne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Revesz, Tamas" sort="Revesz, Tamas" uniqKey="Revesz T" first="Tamas" last="Revesz">Tamas Revesz</name>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Reta Lila Weston Institute of Neurological Studies, University College London</wicri:regionArea>
<wicri:noRegion>University College London</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Queen Square Brain Bank for Neurological Disorders, University College London</wicri:regionArea>
<wicri:noRegion>University College London</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Williams, David R" sort="Williams, David R" uniqKey="Williams D" first="David R." last="Williams">David R. Williams</name>
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<wicri:regionArea>Reta Lila Weston Institute of Neurological Studies, University College London</wicri:regionArea>
<wicri:noRegion>University College London</wicri:noRegion>
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<wicri:regionArea>Queen Square Brain Bank for Neurological Disorders, University College London</wicri:regionArea>
<wicri:noRegion>University College London</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">Australie</country>
<wicri:regionArea>Van Cleef Roet Centre, Monash University, Melbourne</wicri:regionArea>
<wicri:noRegion>Melbourne</wicri:noRegion>
</affiliation>
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<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="2011-08-15">2011-08-15</date>
<biblScope unit="vol">26</biblScope>
<biblScope unit="issue">10</biblScope>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Frontal Lobe (metabolism)</term>
<term>Frontotemporal Dementia (complications)</term>
<term>Frontotemporal Dementia (pathology)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Ophthalmoplegia (complications)</term>
<term>Ophthalmoplegia (pathology)</term>
<term>Posture (physiology)</term>
<term>Sensation Disorders (complications)</term>
<term>Sensation Disorders (pathology)</term>
<term>clinicopathological case</term>
<term>corticobasal degeneration</term>
<term>frontotemporal dementia</term>
<term>progressive supranuclear palsy</term>
<term>tau Proteins (metabolism)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>tau Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Frontotemporal Dementia</term>
<term>Ophthalmoplegia</term>
<term>Sensation Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Frontal Lobe</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Frontotemporal Dementia</term>
<term>Ophthalmoplegia</term>
<term>Sensation Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Posture</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
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<front><div type="abstract" xml:lang="en">A 56‐year‐old man presented with gait disturbance, personality change, and behavioral disturbances. He subsequently developed falls, postural instability, and axial rigidity. The cognitive problems progressed and he developed aphasia and later eye movement abnormalities. He died after 9 years of disease. Experts discuss the syndromal diagnosis and predict the underlying pathology. The pathological diagnosis is given and clinical learning points are considered. © 2011 Movement Disorder Society</div>
</front>
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