Movement Disorders (revue)

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Multiple System Atrophy- Parkinsonism with Slow Progression and Prolonged Survival: A Diagnostic Catch

Identifieur interne : 001110 ( Main/Merge ); précédent : 001109; suivant : 001111

Multiple System Atrophy- Parkinsonism with Slow Progression and Prolonged Survival: A Diagnostic Catch

Auteurs : Igor N. Petrovic [Royaume-Uni] ; Helen Ling [Royaume-Uni, Serbie] ; Yasmine Asi [Serbie] ; Zeshan Ahmed [Serbie] ; Prashanth L. Kukkle [Canada] ; Lili-Naz Hazrati [Canada] ; Anthony E. Lang [Canada] ; Tamas Revesz [Serbie] ; Janice L. Holton [Serbie] ; Andrew Lees (neurologue) [Royaume-Uni, Serbie]

Source :

RBID : Pascal:12-0339928

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English descriptors

Abstract

Background: Multiple system atrophy (MSA) is a neurodegenerative disease leading to severe physical impairment, with a disease duration from onset to death of 6-9 years. Methods: The clinical and neuropathological features of 4 MSA cases with disease duration of 15 years or more were analyzed. Results: All patients presented with parkinsonism and had a mean latency of 11 years before the development of dysautonomia. Mean duration from onset of first symptoms to anterocollis, inspiratory stridor, and dysphagia was 9 years. Despite the limited levodopa response, all patients developed levodopa-induced dyskinesia. Conclusions: Late appearance of dysautonomia is a favorable prognostic factor in MSA-P. Greater awareness of this uncommon "benign" subgroup of MSA will improve diagnostic accuracy and help to more accurately inform treatment options.

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Pascal:12-0339928

Le document en format XML

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<title xml:lang="en" level="a">Multiple System Atrophy- Parkinsonism with Slow Progression and Prolonged Survival: A Diagnostic Catch</title>
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<settlement type="city">Londres</settlement>
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<region type="région" nuts="1">Grand Londres</region>
</placeName>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
<orgName>National Hospital for Neurology and Neurosurgery</orgName>
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<series>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint>
<date when="2012">2012</date>
</imprint>
</series>
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<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Diagnosis</term>
<term>Dysfunction</term>
<term>Multiple system atrophy</term>
<term>Nervous system diseases</term>
<term>Parkinsonism</term>
<term>Survival</term>
<term>Visual hallucination</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Atrophie multisystématisée</term>
<term>Parkinsonisme</term>
<term>Hallucination visuelle</term>
<term>Pathologie du système nerveux</term>
<term>Survie</term>
<term>Diagnostic</term>
<term>Trouble fonctionnel</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">Background: Multiple system atrophy (MSA) is a neurodegenerative disease leading to severe physical impairment, with a disease duration from onset to death of 6-9 years. Methods: The clinical and neuropathological features of 4 MSA cases with disease duration of 15 years or more were analyzed. Results: All patients presented with parkinsonism and had a mean latency of 11 years before the development of dysautonomia. Mean duration from onset of first symptoms to anterocollis, inspiratory stridor, and dysphagia was 9 years. Despite the limited levodopa response, all patients developed levodopa-induced dyskinesia. Conclusions: Late appearance of dysautonomia is a favorable prognostic factor in MSA-P. Greater awareness of this uncommon "benign" subgroup of MSA will improve diagnostic accuracy and help to more accurately inform treatment options.</div>
</front>
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<li>Serbie</li>
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<li>Grand Londres</li>
<li>Ontario</li>
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<settlement>
<li>Londres</li>
<li>Toronto</li>
</settlement>
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<li>National Hospital for Neurology and Neurosurgery</li>
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