Corticobasal manifestations of Creutzfeldt-Jakob disease with D178N-homozygous 129M genotype

Creutzfeldt-Jakob disease (CJD) is a prion disease, usually presented with memory loss, ataxia, dementia, myoclonus, involuntary movements and psychiatric problems. D178N-homozygous 129M genotype has been recognized in the diagnosis of fatal familial insomnia (FFI) globally. Here we report a patient...

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Detalles Bibliográficos
Autores principales: Huang, Yumeng, Jianfang, Ma, Morales, Rodrigo, Tang, Huidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518738/
https://www.ncbi.nlm.nih.gov/pubmed/32946318
http://dx.doi.org/10.1080/19336896.2020.1812367

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518738/
https://www.ncbi.nlm.nih.gov/pubmed/32946318
http://dx.doi.org/10.1080/19336896.2020.1812367

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