Rapidly Progressing Sporadic Creutzfeldt-Jakob Disease Presenting as a Stroke

Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare, fatal human prion disease that is characterized by progressive dementia and neurologic degeneration. It can mimic multiple other neurological disorders, and a high index of clinical suspicion is necessary to make a diagnosis. A 74-year-old woman w...

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Detalles Bibliográficos
Autores principales: Oliver, Maxim, Dyke, Lisa, Rico, Alex, Madruga, Mario, Parellada, Jorge, Carlan, Steve J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180273/
https://www.ncbi.nlm.nih.gov/pubmed/30323754
http://dx.doi.org/10.1159/000492613

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180273/
https://www.ncbi.nlm.nih.gov/pubmed/30323754
http://dx.doi.org/10.1159/000492613

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