A case of V180I genetic Creutzfeldt-Jakob disease presenting with conspicuous facial mimicry

Although there have been no reports of facial mimicry in patients with Creutzfeldt-Jakob disease (CJD), we encountered a patient with genetic CJD with prion protein gene codon 180 mutation (V180I gCJD) who apparently showed this interesting clinical finding. The patient was an 87-year-old Japanese w...

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Detalles Bibliográficos
Autores principales: Iwasaki, Yasushi, Mori, Keiko, Ito, Masumi, Kawai, Yoshinari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746545/
https://www.ncbi.nlm.nih.gov/pubmed/31387445
http://dx.doi.org/10.1080/19336896.2019.1651181

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746545/
https://www.ncbi.nlm.nih.gov/pubmed/31387445
http://dx.doi.org/10.1080/19336896.2019.1651181

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