A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset

Genetic Creutzfeldt-Jakob disease (gCJD) with a mutation in codon 180 of the prion protein gene (V180I gCJD) is the most common form of gCJD in Japan, but only a few cases have been reported in Europe and the United States. It is clinically characterized by occurring in the elderly and presenting as...

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Detalles Bibliográficos
Autores principales: Nomura, Taichi, Iwata, Ikuko, Naganuma, Ryoji, Matsushima, Masaaki, Satoh, Katsuya, Kitamoto, Tetsuyuki, Yabe, Ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518757/
https://www.ncbi.nlm.nih.gov/pubmed/32938301
http://dx.doi.org/10.1080/19336896.2020.1823179

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518757/
https://www.ncbi.nlm.nih.gov/pubmed/32938301
http://dx.doi.org/10.1080/19336896.2020.1823179

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