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다계통위축 임상표현형으로 발현한 2형척수소뇌실조A Patient with Spinocerebellar Ataxia 2 Presenting with Multiple System Atrophy
- Issue Date
- Feb-2020
- Publisher
- 대한신경과학회
- Keywords
- Spinocerebellar ataxias; Multiple system atrophy
- Citation
- 대한신경과학회지, v.38, no.1, pp 33 - 36
- Pages
- 4
- Journal Title
- 대한신경과학회지
- Volume
- 38
- Number
- 1
- Start Page
- 33
- End Page
- 36
- ISSN
- 1225-7044
- Abstract
- Spinocerebellar 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.
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