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TARDBP Mutation Associated with Semantic Variant Primary Progressive Aphasia, Case Report and Review of the Literature

Marta González‐Sánchez, Verónica Puertas‐Martín, Jesús Esteban‐Pérez, Alberto García‐Redondo, Daniel Borrego‐Hernández, Antonio Méndez-Guerrero, Sara Llamas‐Velasco,Alejandro Herrero-San Martín,Pilar Cordero-Vázquez, M. C. Herrero-Manso,D A Pérez-Martínez, Alberto Villarejo‐Galende

Neurocase(2018)

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摘要
Semantic variant primary progressive aphasia (svPPA) is a clinical syndrome included in the frontotemporal dementia (FTD) spectrum. Unlike other forms of FTD, it is sporadic in the majority of cases and not commonly associated with motor neuron disease (MND). We describe a case of svPPA associated with MND in the same family, due to a mutation of the transactive response DNA binding protein (TARDBP) gene, and review the literature.
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