A Patient with Spinocerebellar Ataxia 2 Presenting with Multiple System Atrophy
Journal of the Korean Neurological Association
;
: 33-36, 2020.
Article
| WPRIM
| ID: wpr-834824
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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Indice:
WPRIM (Pacifique occidental)
Texte intégral:
Journal of the Korean Neurological Association
Année:
2020
Type:
Article
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