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다계통위축 임상표현형으로 발현한 2형척수소뇌실조

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dc.contributor.author김용성-
dc.contributor.author이상진-
dc.contributor.author신혜원-
dc.date.available2020-04-10T05:20:07Z-
dc.date.issued2020-02-
dc.identifier.issn1225-7044-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/38240-
dc.description.abstractSpinocerebellar ataxia type-2 (SCA2) is an autosomal dominant cerebellar ataxia that occurs due to expanded CAG trinucleotide repeats in the ATXN2 gene. Clinical features of parkinsonism in SCA2 vary from phenotypes of levodopa-responsive parkinsonism to multiple system atrophy. We described a patient with SCA2 presenting typical clinical manifestations of multiple system atrophy-c type with levodopa responsive parkinsonism whose dopamine transporter (DAT) image showed atypically reduced DAT uptake in in the striatum.-
dc.format.extent4-
dc.language한국어-
dc.language.isoKOR-
dc.publisher대한신경과학회-
dc.title다계통위축 임상표현형으로 발현한 2형척수소뇌실조-
dc.title.alternativeA Patient with Spinocerebellar Ataxia 2 Presenting with Multiple System Atrophy-
dc.typeArticle-
dc.identifier.bibliographicCitation대한신경과학회지, v.38, no.1, pp 33 - 36-
dc.identifier.kciidART002556043-
dc.description.isOpenAccessN-
dc.citation.endPage36-
dc.citation.number1-
dc.citation.startPage33-
dc.citation.title대한신경과학회지-
dc.citation.volume38-
dc.identifier.urlhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002556043-
dc.publisher.location대한민국-
dc.subject.keywordAuthorSpinocerebellar ataxias-
dc.subject.keywordAuthorMultiple system atrophy-
dc.description.journalRegisteredClasskci-
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의과대학 (의학부(임상-서울))
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