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

Internet

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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