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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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| Publicat a: | BMJ Case Rep |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Publishing Group
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6768346/ https://ncbi.nlm.nih.gov/pubmed/31551319 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-230535 |
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