QR Code

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...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Anita S. Bahbah, Esra’a O. Kurdi, Darwish M. Mosameh, Baraa M.M. Sharawi, Mohammed Damrah
Format: Artigo
Langue:Inglês
Publié: BMC 2026-02-01
Collection:BMC Neurology
Sujets:
Accès en ligne:https://doi.org/10.1186/s12883-025-04622-6
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!