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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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Principais autores: Anita S. Bahbah, Esra’a O. Kurdi, Darwish M. Mosameh, Baraa M.M. Sharawi, Mohammed Damrah
פורמט: Artigo
שפה:Inglês
יצא לאור: BMC 2026-02-01
סדרה:BMC Neurology
נושאים:
Creutzfeldt–Jakob disease
Neurodegenerative
Sporadic
גישה מקוונת:https://doi.org/10.1186/s12883-025-04622-6
תגים: הוספת תג
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