Creutzfeldt–Jakob Disease with a Five-Year Clinical Course, Multicentric Cerebellar Prion Plaques and Prior History of Biopsy-Proven Primary Angiitis of the Central Nervous System: A Case for Iatrogenic Exposure?

Creutzfeldt–Jakob disease (CJD) is a rapidly progressive neurodegenerative disease that can arise spontaneously, genetically, or be acquired through iatrogenic exposure. Most patients die within a year of symptom onset. It is rare, affecting 1–2 per million per year, and the majority of cases are sp...

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Detalles Bibliográficos
Autores principales: Jeon, Kristina, Joseph, Jeffrey T., Jansen, Gerard H., Peterson, Anne, Knox, J. David, Sim, Valerie L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763133/
https://www.ncbi.nlm.nih.gov/pubmed/33302561
http://dx.doi.org/10.3390/v12121411

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763133/
https://www.ncbi.nlm.nih.gov/pubmed/33302561
http://dx.doi.org/10.3390/v12121411

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