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Genetic prion diseases presenting as frontotemporal dementia: clinical features and diagnostic challenge

BACKGROUND: To elucidate the clinical and ancillary features of genetic prion diseases (gPrDs) presenting with frontotemporal dementia (FTD) to aid early identification. METHODS: Global data of gPrDs presenting with FTD caused by prion protein gene mutations were collected from literature review and...

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Detalles Bibliográficos
Autores principales:	Chen, Zhongyun, Chu, Min, Liu, Li, Zhang, Jing, Kong, Yu, Xie, Kexin, Cui, Yue, Ye, Hong, Li, Junjie, Wang, Lin, Wu, Liyong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2022
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245249/ https://www.ncbi.nlm.nih.gov/pubmed/35768878 http://dx.doi.org/10.1186/s13195-022-01033-4

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