Unusual nocturnal motor restlessness in a patient with spinocerebellar ataxia 3
Identifieur interne : 000390 ( France/Analysis ); précédent : 000389; suivant : 000391Unusual nocturnal motor restlessness in a patient with spinocerebellar ataxia 3
Auteurs : Imad Ghorayeb [France] ; Federica Provini [Italie] ; Bernard Bioulac [France] ; François Tison [France]Source :
- Movement Disorders [ 0885-3185 ] ; 2005-07.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Female, Human, Humans, Joseph disease, Machado-Joseph Disease (complications), Machado–Joseph disease, Nervous system diseases, Nocturnal Myoclonus Syndrome (etiology), Parasomnia, Polysomnography, Polysomnography (methods), Sleep disorder, Spinocerebellar ataxia, parasomnia, polysomnography, sleep disorders, spinocerebellar ataxia type 3.
- MESH :
- complications : Machado-Joseph Disease.
- etiology : Nocturnal Myoclonus Syndrome.
- methods : Polysomnography.
- Adult, Female, Humans.
Abstract
Video‐polysomnographic monitoring of a female patient with spinocerebellar ataxia 3 (SCA‐3) in whom rapid eye movement (REM) sleep behavior disorder was clinically suspected demonstrated recurrent episodes of unusual nocturnal motor restlessness occurring during non‐REM sleep and severely disturbing both the patient and her bed partner's sleep. Even if nocturnal manifestations are common features of SCA‐3 and increasingly recognized, such a case has never been reported before. We discuss this peculiar movement disorder as a particular manifestation of the wide spectrum of parasomnias occurring in such a rare neurodegenerative disease. © 2005 Movement Disorder Society
Url:
DOI: 10.1002/mds.20415
Affiliations:
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ISTEX:553A56084535C6F42E885E30306835062CBEB777Le document en format XML
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Even if nocturnal manifestations are common features of SCA‐3 and increasingly recognized, such a case has never been reported before. 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