Sporadic MM-1 Type Creutzfeldt-Jakob Disease With Hemiballic Presentation and No Cognitive Impairment Until Death: How New NCJDRSU Diagnostic Criteria May Allow Early Diagnosis

Sporadic Creutzfeldt-Jakob disease is the most common human prion disorder. Although associated with heterogeneous clinical phenotypes, its distinctive feature is the presence of a rapidly progressive multidomain cognitive impairment. We describe the atypical case of a patient affected by sporadic M...

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Detalles Bibliográficos
Autores principales: Saraceno, Lorenzo, Ricigliano, Vito A. G., Cavalli, Michele, Cagol, Alessandro, Bosco, Giovanna, Moda, Fabio, Caroppo, Paola, Meola, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134320/
https://www.ncbi.nlm.nih.gov/pubmed/30233486
http://dx.doi.org/10.3389/fneur.2018.00739

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134320/
https://www.ncbi.nlm.nih.gov/pubmed/30233486
http://dx.doi.org/10.3389/fneur.2018.00739

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