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Disturbance of rapid eye movement sleep in spinocerebellar ataxia type 2

Identifieur interne : 004C36 ( Main/Merge ); précédent : 004C35; suivant : 004C37

Disturbance of rapid eye movement sleep in spinocerebellar ataxia type 2

Auteurs : Sylvia M. Boesch [Autriche] ; Birgit Frauscher [Autriche] ; Elisabeth Brandauer [Autriche] ; Gregor K. Wenning [Autriche] ; Birgit Högl [Autriche] ; Werner Poewe [Autriche]

Source :

Movement disorders [ 0885-3185 ] ; 2006.

RBID : Pascal:06-0538602

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Trouble sommeil, Trouble comportement, Sommeil paradoxal, Ataxie spinocérébelleuse, Atonie, Polysomnographie, Mouvement périodique des jambes.

English descriptors

KwdEn :
- Atonia, Behavioral disorder, Nervous system diseases, Peridoc leg movement, Polysomnography, Rapid eye movement sleep, Sleep disorder, Spinocerebellar ataxia.

Abstract

Five genetically confirmed spinocerebellar ataxia type 2 (SCA2) patients were admitted to our sleep laboratory for two all-night video-polysomnographies. A standard montage was used, including electroencephalography, vertical and horizontal electrooculography, electromyography of mental, submental, and tibialis anterior muscles, and respiratory monitoring. Four of five SCA2 patients had insufficient muscle atonia during rapid eye movement (REM) sleep. All patients exhibited myoclonic jerks during REM sleep, while elaborated behavior was not observed in the video. Abnormal motor control during sleep with periodic leg movements and REM sleep without atonia occurs frequently in SCA2. This finding may reflect a dysfunction of dopaminergic and/or brainstem and cerebellar outflow pathways.

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Pascal:06-0538602

Le document en format XML

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<front><div type="abstract" xml:lang="en">Five genetically confirmed spinocerebellar ataxia type 2 (SCA2) patients were admitted to our sleep laboratory for two all-night video-polysomnographies. A standard montage was used, including electroencephalography, vertical and horizontal electrooculography, electromyography of mental, submental, and tibialis anterior muscles, and respiratory monitoring. Four of five SCA2 patients had insufficient muscle atonia during rapid eye movement (REM) sleep. All patients exhibited myoclonic jerks during REM sleep, while elaborated behavior was not observed in the video. Abnormal motor control during sleep with periodic leg movements and REM sleep without atonia occurs frequently in SCA2. This finding may reflect a dysfunction of dopaminergic and/or brainstem and cerebellar outflow pathways.</div>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Disturbance of rapid eye movement sleep in spinocerebellar ataxia type 2

Disturbance of rapid eye movement sleep in spinocerebellar ataxia type 2

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