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Hallervorden-Spatz syndrome: a rare cause of extrapyramidal manifestations

Hallervorden-Spatz syndrome is a rare neurodegenerative disease of autosomal recessive inheritance which presents in childhood or early adulthood with dystonia, dysarthria, rigidity and choreoathetosis. Here we present an unusual case of atypical Hallervorden-Spatz syndrome with onset during adolesc...

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書目詳細資料
Main Authors: Vinod, KV, Giridharan, S, Dutta, TK
格式: Artigo
語言:Inglês
出版: Indian Academy of Neurosciences 2011
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4116949/
https://ncbi.nlm.nih.gov/pubmed/25205940
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5214/ans.0972.7531.11183012
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