Movement Disorders (revue)

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Association of chorea and motor neuron disease

Identifieur interne : 006894 ( Main/Merge ); précédent : 006893; suivant : 006895

Association of chorea and motor neuron disease

Auteurs : Pierre-Francois Pradat [France] ; Francois Salachas [France] ; Stéphanie Cartalat-Carel [France] ; Lucette Lacomblez [France] ; Nathalie Patte [France] ; Nadine Leforestier [France] ; Véronique Gaura [France] ; Vincent Meininger [France]

Source :

RBID : Pascal:02-0312612

Descripteurs français

English descriptors

Abstract

Amyotrophic lateral sclerosis (ALS) is classically characterized by the presence of symptoms or signs of upper and lower motor neuron impairment and sparing of other neuronal systems.1 We report on a patient who was primarily diagnosed as typical ALS and developed chorea 10 years after the onset of motor neuron signs.

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Pascal:02-0312612

Le document en format XML

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<title level="j" type="main">Movement disorders</title>
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<term>Amyotrophic lateral sclerosis</term>
<term>Case study</term>
<term>Chorea</term>
<term>Concomitant disease</term>
<term>Differential diagnostic</term>
<term>Human</term>
<term>Motor neuron disease</term>
<term>Nuclear magnetic resonance imaging</term>
<term>Video recording</term>
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<keywords scheme="Pascal" xml:lang="fr">
<term>Chorée syndrome</term>
<term>Neurone moteur maladie</term>
<term>Sclérose latérale amyotrophique</term>
<term>Imagerie RMN</term>
<term>Etude cas</term>
<term>Diagnostic différentiel</term>
<term>Association morbide</term>
<term>Homme</term>
<term>Enregistrement vidéo</term>
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<div type="abstract" xml:lang="en">Amyotrophic lateral sclerosis (ALS) is classically characterized by the presence of symptoms or signs of upper and lower motor neuron impairment and sparing of other neuronal systems.
<sup>1</sup>
We report on a patient who was primarily diagnosed as typical ALS and developed chorea 10 years after the onset of motor neuron signs.</div>
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