Case Report: Genetic Creutzfeldt–Jakob Disease With a G114V Mutation and One Octapeptide Repeat Deletion as a Mimic of Frontotemporal Dementia
Genetic Creutzfeldt–Jakob disease (gCJD) characterized by mutations in the prion protein (PrP) gene (PRNP) contributes to approximately 10–15% of the overall human prion diseases. Here, we report a rare mutation in the PRNP gene in a Han-Chinese family. A 36-year-old man initiated with anxiety and d...
Main Authors: | Xue Lin, Yichen Xu, Zhen Zhen, Kang Xiao, Xu Chen, Jigang Yang, Hongzhi Guan, Qi Shi, Xiaoping Dong, Jiawei Wang, Yanjun Guo |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-06-01
|
Series: | Frontiers in Neurology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fneur.2022.888309/full |
Similar Items
-
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion
by: Nicholas Brennecke, et al.
Published: (2021-09-01) -
Creutzfeldt-Jakob disease
by: Lin WANG, et al.
Published: (2013-01-01) -
Creutzfeldt-Jakob disease: current issues (review)
by: A. V. Peresedova, et al.
Published: (2017-02-01) -
Novel prion mutation (p.Tyr225Cys) in a Korean patient with atypical Creutzfeldt–Jakob disease
by: Bagyinszky E, et al.
Published: (2019-08-01) -
The first reported case of Creutzfeldt‐Jakob disease from Nepal
by: Himal Kharel, et al.
Published: (2020-01-01)