Cargando…
Creutzfeldt–Jakob disease: A case report and differential diagnoses
Although sporadic Creutzfeldt–Jakob disease is a rare neurodegenerative disease and often difficult to diagnose at the earliest onset, meticulous clinical examination, electroencephalography, and neuroimaging findings will help in diagnosis.
Autores principales: | Raut, Akash, Thapa, Anjila, Shrestha, Ashish, Saud, Kamal, Rajbhandari, Reema, Katwal, Shailendra |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364331/ https://www.ncbi.nlm.nih.gov/pubmed/35957791 http://dx.doi.org/10.1002/ccr3.6239 |
Ejemplares similares
-
Sporadic Creutzfeldt‐Jakob disease: A case report and review of literature
por: Ojha, Rajeev, et al.
Publicado: (2020) -
Creutzfeldt-Jakob disease: A case report
por: Salehian, Razieh, et al.
Publicado: (2021) -
Rarely fast progressive memory loss diagnosed as Creutzfeldt-Jakob disease: A case report
por: Xu, Yong-Wei, et al.
Publicado: (2021) -
The first reported case of Creutzfeldt‐Jakob disease from Nepal
por: Kharel, Himal, et al.
Publicado: (2019) -
Creutzfeldt–Jakob Disease with Stroke-Like Symptoms: Case report
por: Tosunoğlu, Bünyamin, et al.
Publicado: (2022)