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Rare histotype of sporadic Creutzfeldt-Jakob disease, clinically suspected as corticobasal degeneration
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare neurodegenerative disease that can mimic other neurological disorders. We present a case of sCJD in a 64-year-old man that presented with corticobasal syndrome and survived for 3 years. He presented initially with dementia, hemiparkinsonism and ali...
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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/PMC6424260/ https://ncbi.nlm.nih.gov/pubmed/30850568 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2018-228305 |
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