Unusual presentations in patients with E200K familial Creutzfeldt-Jakob Disease

BACKGROUND AND PROPOSE: Familial Creutzfeldt-Jakob disease (fCJD) in Jews of Libyan ancestry is caused by an E200K mutation in the PRNP gene. The typical presenting symptoms include cognitive decline, behavioral changes and gait disturbances, however some patients may have an unusual presentation su...

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Publicado en:Eur J Neurol
Autores principales: Cohen, Oren S., Kimiagar, Itzhak, Korczyn, Amos D., Nitsan, Zeev, Appel, Shmuel, Hoffmann, Chen, Rosenmann, Hanna, Kahana, Esther, Chapman, Joab
Formato: Artigo
Lenguaje:Inglês
Publicado: 2016
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4833540/
https://ncbi.nlm.nih.gov/pubmed/26806765
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ene.12955
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