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Case report of a patient with unclassified tauopathy with molecular and neuropathological features of both progressive supranuclear palsy and corticobasal degeneration

Abstract Progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) are distinct clinicopathological subtypes of frontotemporal lobar degeneration. They both have atypical parkinsonism, and they usually have distinct clinical features. The most common clinical presentation of PSP is Ri...

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Principais autores: Shunsuke Koga, Michael A. Metrick, Lawrence I. Golbe, Alessia Santambrogio, Minji Kim, Alexandra I. Soto-Beasley, Ronald L. Walton, Matthew C. Baker, Cristhoper Fernandez De Castro, Michael DeTure, David Russell, Bradford A. Navia, Christine Sandiego, Owen A. Ross, Michele Vendruscolo, Byron Caughey, Dennis W. Dickson
Format: Artigo
Sprog:Inglês
Udgivet: BMC 2023-06-01
Serier:Acta Neuropathologica Communications
Fag:
Progressive supranuclear palsy
Corticobasal degeneration
Tauopathy
Tufted astrocyte
Astrocytic plaque
Tau PET
Online adgang:https://doi.org/10.1186/s40478-023-01584-z
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