Literature DB >> 18706660

Atypical presentation of Creutzfeldt-Jakob disease: the first Italian case associated with E196K mutation in the PRNP gene.

F Clerici1, A Elia, F Girotti, P Contri, C Mariani, F Tagliavini, G Di Fede.   

Abstract

Genetic Creutzfeldt-Jakob disease (gCJD) is caused by a range of mutations in the prion protein gene (PRNP). We describe the first Italian case of gCJD associated with the rare PRNP E196K mutation. The disease showed an atypical presentation featuring dementia without motor signs in a 75-year-old woman. The case lacked both a known family history of a similar neurological disease and the typical EEG pattern; it was misdiagnosed as frontotemporal dementia. The present case emphasizes that vigilance must be kept high to avoid missing gCJD cases falling outside a typical phenotypical presentation and a known family history, especially in the elderly, in whom an alternative, more common, but incorrect diagnosis may be made.

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Year:  2008        PMID: 18706660     DOI: 10.1016/j.jns.2008.06.036

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  9 in total

1.  A Chinese Creutzfeldt-Jakob disease patient with E196K mutation in PRNP.

Authors:  Qi Shi; Cao Chen; Xiao-Nan Song; Chen Gao; Chan Tian; Wei Zhou; Xu-Hua Song; Lai-Shun Yao; Jun Han; Xiao-Ping Dong
Journal:  Prion       Date:  2011-04-01       Impact factor: 3.931

Review 2.  Genetic prion diseases presenting as frontotemporal dementia: clinical features and diagnostic challenge.

Authors:  Zhongyun Chen; Min Chu; Li Liu; Jing Zhang; Yu Kong; Kexin Xie; Yue Cui; Hong Ye; Junjie Li; Lin Wang; Liyong Wu
Journal:  Alzheimers Res Ther       Date:  2022-06-29       Impact factor: 8.823

3.  Rare E196A mutation in PRNP gene of 3 Chinese patients with Creutzfeldt-Jacob disease.

Authors:  Qi Shi; Wei Zhou; Cao Chen; Bao-Yun Zhang; Kang Xiao; Yuan Wang; Xiao-Ping Dong
Journal:  Prion       Date:  2016-07-03       Impact factor: 3.931

Review 4.  Translational Research in Alzheimer's and Prion Diseases.

Authors:  Giuseppe Di Fede; Giorgio Giaccone; Mario Salmona; Fabrizio Tagliavini
Journal:  J Alzheimers Dis       Date:  2018       Impact factor: 4.472

5.  Novel prion mutation (p.Tyr225Cys) in a Korean patient with atypical Creutzfeldt-Jakob disease.

Authors:  Eva Bagyinszky; YoungSoon Yang; Vo Van Giau; Young Chul Youn; Seong Soo A An; SangYun Kim
Journal:  Clin Interv Aging       Date:  2019-08-02       Impact factor: 4.458

6.  Characteristics of Chinese patients with genetic CJD who have E196A or E196K mutation in PRNP: comparative analysis of patients identified in the Chinese National CJD Surveillance System.

Authors:  Qi Shi; Kang Xiao; Cao Chen; Wei Zhou; Li-Ping Gao; Yue-Zhang Wu; Yuan Wang; Chao Hu; Chen Gao; Xiao-Ping Dong
Journal:  BMJ Open       Date:  2021-11-15       Impact factor: 2.692

7.  Alterations of Striatal Subregions in a Prion Protein Gene V180I Mutation Carrier Presented as Frontotemporal Dementia With Parkinsonism.

Authors:  Zhongyun Chen; Jinghong Ma; Li Liu; Shuying Liu; Jing Zhang; Min Chu; Zhen Wang; Piu Chan; Liyong Wu
Journal:  Front Aging Neurosci       Date:  2022-04-15       Impact factor: 5.702

Review 8.  Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases.

Authors:  Eva Bagyinszky; Vo Van Giau; Young Chul Youn; Seong Soo A An; SangYun Kim
Journal:  Neuropsychiatr Dis Treat       Date:  2018-08-14       Impact factor: 2.570

Review 9.  Cellular Prion Protein (PrPc): Putative Interacting Partners and Consequences of the Interaction.

Authors:  Hajar Miranzadeh Mahabadi; Changiz Taghibiglou
Journal:  Int J Mol Sci       Date:  2020-09-25       Impact factor: 5.923

  9 in total

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