Sporadic Creutzfeldt–Jakob disease in Palestine with early ataxia and dysarthria: a case report
Abstract Creutzfeldt–Jakob disease (CJD) is a rare and fatal neurodegenerative disorder caused by misfolded prion proteins. It progresses inexorably to death once clinical symptoms emerge. Early manifestations are often nonspecific and may mimic other neurological conditions, making diagnosis partic...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMC
2026-02-01
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| Edice: | BMC Neurology |
| Témata: | |
| On-line přístup: | https://doi.org/10.1186/s12883-025-04622-6 |
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