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Comatose within 6 weeks, but still alive after 3 years, Creutzfeldt‐Jakob disease with unusual progression
Creutzfeldt‐Jakob disease (CJD) should still be considered in a patient presenting with rapidly progressive dementia and negative CSF 14‐3‐3 protein and RT‐QulC. Treatable causes of encephalopathy must be ruled out. Neurodegenerative diseases must also be considered.
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303844/ https://www.ncbi.nlm.nih.gov/pubmed/32577246 http://dx.doi.org/10.1002/ccr3.2807 |