Atypical Case of VV1 Creutzfeldt–Jakob Disease Subtype: Case Report

Creutzfeldt–Jakob disease (CJD) is a rare form of rapidly progressive, neurodegenerative disease that results from the misfolding and accumulation of an aberrant, disease-associated prion protein (PrPD). CJD affects 1–1.5 cases per million per year with the sporadic-type accounting for an estimated...

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Detalles Bibliográficos
Autores principales: Carrasco, Adrianna E., Appleby, Brian S., Cali, Ignazio, Okhravi, Hamid R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124891/
https://www.ncbi.nlm.nih.gov/pubmed/35614914
http://dx.doi.org/10.3389/fneur.2022.875370

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124891/
https://www.ncbi.nlm.nih.gov/pubmed/35614914
http://dx.doi.org/10.3389/fneur.2022.875370

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