Movement Disorders (revue)

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Long lasting pure freezing of gait preceding progressive supranuclear palsy: A clinicopathological study

Identifieur interne : 002D68 ( Main/Exploration ); précédent : 002D67; suivant : 002D69

Long lasting pure freezing of gait preceding progressive supranuclear palsy: A clinicopathological study

Auteurs : Yaroslau Compta [Espagne] ; Francesc Valldeoriola [Espagne] ; Eduardo Tolosa [Espagne] ; María Jesús Rey [Espagne] ; María José Martí [Espagne] ; Josep Valls-Solé [Espagne]

Source :

RBID : ISTEX:123F5E6203E34158C63C258691F3DBAF31840EF1

Descripteurs français

English descriptors

Abstract

Primary progressive freezing of gait (PPFG) is the term used to designate an uncommon condition featuring freezing of gait with frequent falls, without bradykinesia, rigidity or tremor, and unresponsive to levodopa. There are very few pathological reports of patients with PPFG in the literature. We report on 2 patients (one with pathological confirmation) diagnosed initially as PPFG and evolving into clinically defined progressive supranuclear palsy (PSP) more than 10 years after onset of symptoms. These 2 cases suggest that PPFG can represent the initial manifestation of a neurodegenerative disease, such as PSP, rather than a differentiated nosological entity. © 2007 Movement Disorder Society

Url:
DOI: 10.1002/mds.21612


Affiliations:


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Le document en format XML

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<term>Disease Progression</term>
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<div type="abstract" xml:lang="en">Primary progressive freezing of gait (PPFG) is the term used to designate an uncommon condition featuring freezing of gait with frequent falls, without bradykinesia, rigidity or tremor, and unresponsive to levodopa. There are very few pathological reports of patients with PPFG in the literature. We report on 2 patients (one with pathological confirmation) diagnosed initially as PPFG and evolving into clinically defined progressive supranuclear palsy (PSP) more than 10 years after onset of symptoms. These 2 cases suggest that PPFG can represent the initial manifestation of a neurodegenerative disease, such as PSP, rather than a differentiated nosological entity. © 2007 Movement Disorder Society</div>
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