MovDisordV3, Main, Merge, bibRecord, 004128

Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy

Identifieur interne : 004128 ( Main/Merge ); précédent : 004127; suivant : 004129

Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy

Auteurs : Bart P. C. Van De Warrenburg [Royaume-Uni, Pays-Bas] ; Carla Cordivari [Royaume-Uni] ; Peter Brown [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]

Source :

Movement disorders [ 0885-3185 ] ; 2007.

RBID : Pascal:07-0314960

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Encéphalopathie, Trismus, Autoimmunité, Myoclonie, Idiopathique, Réflexe, Muscle masticateur, Hyperekplexie.

English descriptors

KwdEn :
- Autoimmunity, Encephalopathy, Hyperekplexia, Idiopathic, Masticatory muscle, Myoclonus, Nervous system diseases, Reflex, Trismus.

Abstract

Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self-limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted.

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Pascal:07-0314960

Le document en format XML

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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy</title>
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<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
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<affiliation wicri:level="3"><inist:fA14 i1="02"><s1>Department of Neurology, Radboud University Nijmegen Medical Centre</s1>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Autoimmunity</term>
<term>Encephalopathy</term>
<term>Hyperekplexia</term>
<term>Idiopathic</term>
<term>Masticatory muscle</term>
<term>Myoclonus</term>
<term>Nervous system diseases</term>
<term>Reflex</term>
<term>Trismus</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term>
<term>Encéphalopathie</term>
<term>Trismus</term>
<term>Autoimmunité</term>
<term>Myoclonie</term>
<term>Idiopathique</term>
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<front><div type="abstract" xml:lang="en">Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self-limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted.</div>
</front>
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<name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name>
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<name sortKey="Cordivari, Carla" sort="Cordivari, Carla" uniqKey="Cordivari C" first="Carla" last="Cordivari">Carla Cordivari</name>
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<country name="Pays-Bas"><region name="Gueldre"><name sortKey="Van De Warrenburg, Bart P C" sort="Van De Warrenburg, Bart P C" uniqKey="Van De Warrenburg B" first="Bart P. C." last="Van De Warrenburg">Bart P. C. Van De Warrenburg</name>
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</record>

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	Movement Disorders (revue)
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Movement Disorders (revue)

Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy

Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri