Movement Disorders (revue)

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Progressive supranuclear palsy-like phenotype associated with bilateral hypoxic-ischemic striopallidal lesions

Identifieur interne : 003A59 ( Main/Exploration ); précédent : 003A58; suivant : 003A60

Progressive supranuclear palsy-like phenotype associated with bilateral hypoxic-ischemic striopallidal lesions

Auteurs : HEE TAE KIM [Royaume-Uni] ; Simon Shields [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Niall Quinn [Royaume-Uni]

Source :

RBID : Pascal:05-0363727

Descripteurs français

English descriptors

Abstract

A progressive supranuclear palsy (PSP)-like syndrome due to vascular or anoxic brain insult is rare. We describe a 65-year-old man with a progressive PSP-like phenotype associated with hypoxic-ischemic bilateral striopallidal lesions, secondary to rupture of and subsequent surgery for a thoracic aortic aneurysm. After early extrapyramidal features, 10 months later he started to fall, and developed levator inhibition. A supranuclear gaze palsy for downgaze was documented 5.5 years after the insult.


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">A progressive supranuclear palsy (PSP)-like syndrome due to vascular or anoxic brain insult is rare. We describe a 65-year-old man with a progressive PSP-like phenotype associated with hypoxic-ischemic bilateral striopallidal lesions, secondary to rupture of and subsequent surgery for a thoracic aortic aneurysm. After early extrapyramidal features, 10 months later he started to fall, and developed levator inhibition. A supranuclear gaze palsy for downgaze was documented 5.5 years after the insult.</div>
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