Parkinsonism in Gerstmann-Sträussler-Scheinker disease: A case report

Background: Autosomal dominant prion diseases of the central nervous system, including Gerstmann-Sträussler-Scheinker disease (GSS), Creutzfeldt-Jakob disease, and fatal familial insomnia, are caused by mutations in the PRNP gene. These conditions exhibit highly variable clinical and pathological fe...

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Bibliografische gegevens
Gepubliceerd in:eNeurologicalSci
Hoofdauteurs: Santiago Poveda, Juan Sebastián Montealegre-Claros, Lina María Lancheros, Maria Alejandra Cruz, Oscar Bernal Pacheco
Formaat: Artikel
Gepubliceerd in: Elsevier 2025-12-01
Onderwerpen:
Gerstmann-Sträussler-Scheinker disease
Spongiform encephalopathies
Prion diseases
Parkinsonism
PRNP mutation
Online toegang:http://www.sciencedirect.com/science/article/pii/S2405650225000413
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http://www.sciencedirect.com/science/article/pii/S2405650225000413

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