Movement Disorders (revue)

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Postural instability, frontotemporal dementia, and ophthalmoplegia: Clinicopathological case

Identifieur interne : 002C22 ( Istex/Corpus ); précédent : 002C21; suivant : 002C23

Postural instability, frontotemporal dementia, and ophthalmoplegia: Clinicopathological case

Auteurs : Francisco Cardoso ; John Hodges ; Andrew H. Evans ; Tamas Revesz ; David R. Williams

Source :

RBID : ISTEX:4F3FB89454FF861F31568290C5FEE64B29C7D3C4

English descriptors

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

Links to Exploration step

ISTEX:4F3FB89454FF861F31568290C5FEE64B29C7D3C4

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<p>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
<i>Movement</i>
Disorder Society</p>
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<b>Relevant conflicts of interest/financial disclosures:</b>
Nothing to report. Full financial disclosures and author roles may be found in the online version of this article.</p>
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<title>Postural instability, frontotemporal dementia, and ophthalmoplegia: Clinicopathological case</title>
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<namePart type="given">Francisco</namePart>
<namePart type="family">Cardoso</namePart>
<namePart type="termsOfAddress">MD, PhD</namePart>
<affiliation>Movement Disorders Unit, Neurology Service, Federal University of Minas Gerais, Belo Horizonte, Brazil</affiliation>
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<name type="personal">
<namePart type="given">John</namePart>
<namePart type="family">Hodges</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Prince of Wales Medical Research Institute, University of New South Wales, Sydney, Australia</affiliation>
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<name type="personal">
<namePart type="given">Andrew H.</namePart>
<namePart type="family">Evans</namePart>
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<affiliation>Department of Neurology, Royal Melbourne Hospital, Melbourne, Australia</affiliation>
<role>
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<name type="personal">
<namePart type="given">Tamas</namePart>
<namePart type="family">Revesz</namePart>
<namePart type="termsOfAddress">MD, FRCPath</namePart>
<affiliation>Reta Lila Weston Institute of Neurological Studies, University College London, United Kingdom</affiliation>
<affiliation>Queen Square Brain Bank for Neurological Disorders, University College London, United Kingdom</affiliation>
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<name type="personal">
<namePart type="given">David R.</namePart>
<namePart type="family">Williams</namePart>
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<affiliation>Reta Lila Weston Institute of Neurological Studies, University College London, United Kingdom</affiliation>
<affiliation>Queen Square Brain Bank for Neurological Disorders, University College London, United Kingdom</affiliation>
<affiliation>Van Cleef Roet Centre, Monash University, Melbourne, Australia</affiliation>
<description>Correspondence: Van Cleef Roet Centre, Monash University (Alfred Hospital Campus), Commercial Rd, Melbourne 3004, Australia</description>
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<abstract 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</abstract>
<note type="additional physical form">Supporting video</note>
<note type="content">*Relevant conflicts of interest/financial disclosures: Nothing to report. Full financial disclosures and author roles may be found in the online version of this article.</note>
<subject lang="en">
<genre>Keywords</genre>
<topic>frontotemporal dementia</topic>
<topic>corticobasal degeneration</topic>
<topic>progressive supranuclear palsy</topic>
<topic>clinicopathological case</topic>
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<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
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<date>2011</date>
<detail type="volume">
<caption>vol.</caption>
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<caption>no.</caption>
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