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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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Detalles Bibliográficos
Autores principales: Vinod, KV, Giridharan, S, Dutta, TK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Academy of Neurosciences 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116949/
https://www.ncbi.nlm.nih.gov/pubmed/25205940
http://dx.doi.org/10.5214/ans.0972.7531.11183012

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