A Corticobasal Syndrome Variant of Familial Creutzfeldt-Jakob Disease with Stroke-Like Onset

Creutzfeldt-Jakob disease (CJD) is an untreatable rare human prion disease characterized by rapidly progressive dementia along with various neurological features, including myoclonus and sometimes other movement disorders. The clinical course is typically insidious and rapid, leading to an early dea...

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Detalles Bibliográficos
Autores principales: Necpál, Ján, Stelzer, Martin, Koščová, Silvia, Patarák, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075606/
https://www.ncbi.nlm.nih.gov/pubmed/27803826
http://dx.doi.org/10.1155/2016/4167391

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