Diagnostic challenge of rapidly progressing sporadic Creutzfeldt-Jakob disease

Antemortem assessment of sporadic Creutzfeldt-Jakob disease (sCJD) can be significantly hampered due to its rarity, low index of clinical suspicion and its non-specific clinical features. We present an atypical case of definitive sCJD. The patient died within 5 weeks of the disease onset. This unusu...

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Detalles Bibliográficos
Autores principales: Kwon, Gi Tae, Kwon, Min Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Rare Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768346/
https://www.ncbi.nlm.nih.gov/pubmed/31551319
http://dx.doi.org/10.1136/bcr-2019-230535

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768346/
https://www.ncbi.nlm.nih.gov/pubmed/31551319
http://dx.doi.org/10.1136/bcr-2019-230535

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