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Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
Ann Neurol 50:812-815, Shan,D.,et al, 2001
See this aricle in Pubmed

Article Abstract
A genetic analysis identified 2 patients, approximately one-tenth of our patients with familial parkinsonism, who had expanded trinucleotide repeats in SCA2 genes. The reduction of 18F-dopa distribution in both the putamen and caudate nucle i confirmed that the nigrostriatal dopaminergic system was involved in parkinsonian patients with SCA2 mutation.
 
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familial
genetic neurologic disorders
L-dopa
Parkinsonism syndrome
sinemet
spinocerebellar ataxia
spinocerebellar ataxia type 2
trinucleotide repeats

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