Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil

Genetic Creutzfeldt-Jakob disease (gCJD) represents less than 15% of CJD cases, and its clinical picture may be either indistinguishable from that of sporadic CJD (sCJD) or be atypical, usually with younger onset and longer duration. We report a case of 59-year old Brazilian man who presented rapidl...

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Detalles Bibliográficos
Autores principales: Smid, Jerusa, Martins, Vilma Regina, Landemberger, Michele Christine, Riva, Daniele, Anghinah, Renato, Nitrini, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação de Neurologia Cognitiva e do Comportamento 2007
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619573/
https://www.ncbi.nlm.nih.gov/pubmed/29213392
http://dx.doi.org/10.1590/s1980-57642008dn10200017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619573/
https://www.ncbi.nlm.nih.gov/pubmed/29213392
http://dx.doi.org/10.1590/s1980-57642008dn10200017

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