Disturbance of rapid eye movement sleep in spinocerebellar ataxia type 2
Identifieur interne : 003481 ( Main/Exploration ); précédent : 003480; suivant : 003482Disturbance 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 ] ; 2006-10.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Adult, Atonia, Behavioral disorder, Chromosome Aberrations, Eye Movements (physiology), Female, Genes, Dominant, Humans, Male, Middle Aged, Muscle Tonus (physiology), Muscle, Skeletal (physiopathology), Nerve Tissue Proteins (genetics), Nervous system diseases, Nocturnal Myoclonus Syndrome (diagnosis), Nocturnal Myoclonus Syndrome (genetics), Peridoc leg movement, Pilot Projects, Polysomnography, REM Sleep Parasomnias (diagnosis), REM Sleep Parasomnias (genetics), REM sleep behavior disorder (RBD), REM sleep without atonia (RWA), Rapid eye movement sleep, Sleep Stages (physiology), Sleep disorder, Spinocerebellar Ataxias (diagnosis), Spinocerebellar Ataxias (genetics), Spinocerebellar ataxia, Video Recording, periodic leg movements (PLM), polysomnography, spinocerebellar ataxia type 2 (SCA2).
- MESH :
- chemical , genetics : Nerve Tissue Proteins.
- diagnosis : Nocturnal Myoclonus Syndrome, REM Sleep Parasomnias, Spinocerebellar Ataxias.
- genetics : Nocturnal Myoclonus Syndrome, REM Sleep Parasomnias, Spinocerebellar Ataxias.
- physiology : Eye Movements, Muscle Tonus, Sleep Stages.
- physiopathology : Muscle, Skeletal.
- Adult, Chromosome Aberrations, Female, Genes, Dominant, Humans, Male, Middle Aged, Pilot Projects, Polysomnography, Video Recording.
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. © 2006 Movement Disorder Society
Url:
DOI: 10.1002/mds.21036
Affiliations:
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<term>Atonia</term>
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<term>Chromosome Aberrations</term>
<term>Eye Movements (physiology)</term>
<term>Female</term>
<term>Genes, Dominant</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Muscle Tonus (physiology)</term>
<term>Muscle, Skeletal (physiopathology)</term>
<term>Nerve Tissue Proteins (genetics)</term>
<term>Nervous system diseases</term>
<term>Nocturnal Myoclonus Syndrome (diagnosis)</term>
<term>Nocturnal Myoclonus Syndrome (genetics)</term>
<term>Peridoc leg movement</term>
<term>Pilot Projects</term>
<term>Polysomnography</term>
<term>REM Sleep Parasomnias (diagnosis)</term>
<term>REM Sleep Parasomnias (genetics)</term>
<term>REM sleep behavior disorder (RBD)</term>
<term>REM sleep without atonia (RWA)</term>
<term>Rapid eye movement sleep</term>
<term>Sleep Stages (physiology)</term>
<term>Sleep disorder</term>
<term>Spinocerebellar Ataxias (diagnosis)</term>
<term>Spinocerebellar Ataxias (genetics)</term>
<term>Spinocerebellar ataxia</term>
<term>Video Recording</term>
<term>periodic leg movements (PLM)</term>
<term>polysomnography</term>
<term>spinocerebellar ataxia type 2 (SCA2)</term>
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<term>REM Sleep Parasomnias</term>
<term>Spinocerebellar Ataxias</term>
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<term>REM Sleep Parasomnias</term>
<term>Spinocerebellar Ataxias</term>
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<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Eye Movements</term>
<term>Muscle Tonus</term>
<term>Sleep Stages</term>
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<term>Chromosome Aberrations</term>
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<term>Genes, Dominant</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Pilot Projects</term>
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<term>Video Recording</term>
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<term>Atonie</term>
<term>Mouvement périodique des jambes</term>
<term>Polysomnographie</term>
<term>Sommeil paradoxal</term>
<term>Système nerveux pathologie</term>
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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. © 2006 Movement Disorder Society</div>
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<name sortKey="Wenning, Gregor K" sort="Wenning, Gregor K" uniqKey="Wenning G" first="Gregor K." last="Wenning">Gregor K. Wenning</name>
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