Genetic Creutzfeldt-Jakob disease shows fatal family insomnia phenotype

We report a case of genetic Creutzfeldt-Jakob disease (gCJD), which has a clinical phenotype that is highly similar to Fatal Family Insomnia (FFI) and has a triad of Wernicke-Korsakoff syndrome (WKs) at the developmental stage of the disease. The 51-year-old male complained of sleep disorder and imb...

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Detalles Bibliográficos
Autores principales: Chen, Bin, Zhang, Shan, Xiao, Ying, Wu, yingman, Tang, Weiting, Yan, Limin, Zhang, Zhengxue, Qin, Shengquan, Dai, Mingming, You, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425754/
https://www.ncbi.nlm.nih.gov/pubmed/34486485
http://dx.doi.org/10.1080/19336896.2021.1968291

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425754/
https://www.ncbi.nlm.nih.gov/pubmed/34486485
http://dx.doi.org/10.1080/19336896.2021.1968291

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