Progressive parkinsonism, oculomotor abnormalities and autonomic dysfunction: Clinicopathological case
Identifieur interne : 001452 ( Main/Exploration ); précédent : 001451; suivant : 001453Progressive parkinsonism, oculomotor abnormalities and autonomic dysfunction: Clinicopathological case
Auteurs : Giovanni Fabbrini [Italie] ; Marcello Merello [Argentine] ; Andrew H. Evans [Australie] ; Andrew Lees (neurologue) [Royaume-Uni] ; Janice Holton [Royaume-Uni] ; David R. Williams [Royaume-Uni, Australie]Source :
- Movement Disorders [ 0885-3185 ] ; 2011-02-15.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Autonomic Nervous System Diseases (complications), Autonomic Nervous System Diseases (pathology), Disease Progression, Dysfunction, Female, Humans, Inclusion Bodies (pathology), MSA, Middle Aged, Nervous system diseases, Ocular Motility Disorders (complications), Ocular Motility Disorders (pathology), PSP, Parkinsonian Disorders (complications), Parkinsonian Disorders (pathology), Parkinsonism, Putamen (pathology), clinicopathological case.
- MESH :
Abstract
A 59‐year‐old woman presented with asymmetric parkinsonism that was not‐responsive to Levodopa therapy. She developed early falls, postural instability, and moderately severe autonomic dysfunction. Eye movement abnormalities were reported 2 years after her first symptoms, and she eventually developed anterocollis. 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.23302
Affiliations:
- Argentine, Australie, Italie, Royaume-Uni
- Angleterre, Grand Londres
- Londres
- National Hospital for Neurology and Neurosurgery
Links toward previous steps (curation, corpus...)
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Le document en format XML
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<front><div type="abstract" xml:lang="en">A 59‐year‐old woman presented with asymmetric parkinsonism that was not‐responsive to Levodopa therapy. She developed early falls, postural instability, and moderately severe autonomic dysfunction. Eye movement abnormalities were reported 2 years after her first symptoms, and she eventually developed anterocollis. 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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<li>Royaume-Uni</li>
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<li>Grand Londres</li>
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<country name="Argentine"><noRegion><name sortKey="Merello, Marcello" sort="Merello, Marcello" uniqKey="Merello M" first="Marcello" last="Merello">Marcello Merello</name>
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<country name="Australie"><noRegion><name sortKey="Evans, Andrew H" sort="Evans, Andrew H" uniqKey="Evans A" first="Andrew H." last="Evans">Andrew H. Evans</name>
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<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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<country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Lees, Andrew J" sort="Lees, Andrew J" uniqKey="Lees A" first="Andrew J." last="Lees">Andrew Lees (neurologue)</name>
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<name sortKey="Holton, Janice" sort="Holton, Janice" uniqKey="Holton J" first="Janice" last="Holton">Janice Holton</name>
<name sortKey="Holton, Janice" sort="Holton, Janice" uniqKey="Holton J" first="Janice" last="Holton">Janice Holton</name>
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<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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