Sporadic Creutzfeldt‐Jakob disease: A case report and review of literature
Abstract Creutzfeldt‐Jakob Disease is a rare neurodegenerative disease and earlier diagnosis is usually difficult. Combining clinical features with electroencephalogram, laboratory parameters, and neuroimaging findings will facilitate the diagnosis.
Main Authors: | Rajeev Ojha, Gaurav Nepal, Sujan Jamarkattel, Bikram Prasad Gajurel, Ragesh Karn, Reema Rajbhandari |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2020-11-01
|
Series: | Clinical Case Reports |
Subjects: | |
Online Access: | https://doi.org/10.1002/ccr3.3131 |
Similar Items
-
Differentiation of Prions from L-type BSE versus Sporadic Creutzfeldt-Jakob Disease
by: Simon Nicot, et al.
Published: (2012-12-01) -
Creutzfeldt-Jakob disease: a survey of 14 patients Doença de Creutzfeldt-Jakob: relato de 14 pacientes
by: Paulo E. Marchiori, et al.
Published: (1996-12-01) -
Creutzfeldt-Jacob disease: An autopsy case report in tertiary care hospital
by: Nitin M Gadgil, et al.
Published: (2012-01-01) -
The first reported case of Creutzfeldt‐Jakob disease from Nepal
by: Himal Kharel, et al.
Published: (2020-01-01) -
Creutzfeldt–Jakob disease in the Republic of Sakha (Yakutia)
by: T. E. Popova, et al.
Published: (2020-04-01)