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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Indian Academy of Neurosciences
2011
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| 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 |