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dc.contributor.author최경규-
dc.contributor.author구혜수-
dc.date.accessioned2018-12-14T16:31:15Z-
dc.date.available2018-12-14T16:31:15Z-
dc.date.issued2018-
dc.identifier.issn1011-8934-
dc.identifier.otherOAK-22413-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/247864-
dc.description.abstractDentatorubropallidoluysian atrophy (DRPLA) is a neurodegenerative disease caused by an expansion of a cytosine-adenine-guanine (CAG) repeat encoding a polyglutamine tract in the atrophin-1 protein. Unlike other CAG repeat diseases, sleep related problems have not been reported in patients with DRPLA. There was a 65-year-old man and his family with DRPLA. They suffered from seizure, gait disturbance, and cognitive decline. The patients commonly showed dream enacting sleep disorder, insomnia. The results from overnight polysomnography showed rapid eye movement (REM) without atonia in patients with DRPLA. The man died 2 years after diagnosis and was subjected for brain autopsy. We report REM sleep behavior disorders in patients with DRPLA confirmed with polysomnography with pathological description of the patient. © 2018 The Korean Academy of Medical Sciences.-
dc.languageEnglish-
dc.publisherKorean Academy of Medical Science-
dc.subjectCerebellar ataxia-
dc.subjectDentatorubropallidoluysian Atrophy-
dc.titleSleep related problems as a nonmotor symptom of dentatorubropallidoluysian atrophy-
dc.typeArticle-
dc.relation.issue17-
dc.relation.volume33-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.indexKCI-
dc.relation.journaltitleJournal of Korean Medical Science-
dc.identifier.doi10.3346/jkms.2018.33.e130-
dc.identifier.wosidWOS:000432464200005-
dc.identifier.scopusid2-s2.0-85046091421-
dc.author.googleKim H.-
dc.author.googleYun J.Y.-
dc.author.googleChoi K.-G.-
dc.author.googleKoo H.-
dc.author.googleHan H.J.-
dc.contributor.scopusid최경규(24472766200;37664619600)-
dc.contributor.scopusid구혜수(7102121023;57217717081;56612832400)-
dc.date.modifydate20230616142633-


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