Progressive supranuclear palsy phenotype as an atypical clinical presentation of Creutzfeldt-Jakob disease: A case report and review of the literature

Creutzfeldt-Jakob disease (CJD) is a rare, rapidly progressive neurodegenerative disorder, characterized by the accumulation of abnormal prion proteins in the brain. While CJD has some typical clinical features, its presentation can be quite heterogeneous, particularly in the early stages of the dis...

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Bibliographic Details
Main Authors: Matteo Costanzo, Flavia Aiello, Anna Poleggi, Pietro Li Voti, Giovanni Fabbrini, Daniele Belvisi
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Clinical Parkinsonism & Related Disorders
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2590112524000161