Literature DB >> 10778571

Stroke like presentation of Creutzfeldt Jakob disease: an unusual variant.

A Panagariya1, R S Jain, A K Sharma.   

Abstract

Creutzfeldt-Jakob disease (CJD) is a degenerative process of the brain, induced by novel infectious agent or prion, and is usually characterized by a rapidly progressive dementia in association with myoclonus. However different patterns of disease presentation have been identified. The authors describe three probable cases of CJD. None of them had positive family history or any known modes of iatrogenic transmission. Interestingly, all the cases presented like a stroke. This is the first series of CJD cases from this part of country.

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Year:  1999        PMID: 10778571

Source DB:  PubMed          Journal:  J Assoc Physicians India        ISSN: 0004-5772


  4 in total

Review 1.  Rapidly progressive dementia.

Authors:  Michael D Geschwind; Huidy Shu; Aissa Haman; James J Sejvar; Bruce L Miller
Journal:  Ann Neurol       Date:  2008-07       Impact factor: 10.422

2.  Case series of Creutzfeldt-Jakob disease in a third-level hospital in Quito.

Authors:  Germaine Eleanor Torres Herrán; Andrés Damián Ortega Heredia; Braulio Martinez Burbano; Marcos Serrano-Dueñas; María Angélica Ortiz Yepez; Raúl Alberto Barrera Madera; Luis Alfredo Masabanda Campaña; Guillermo David Baño Jiménez; Denny Maritza Santos Saltos; Edgar Patricio Correa Díaz
Journal:  BMC Neurol       Date:  2018-04-27       Impact factor: 2.474

3.  Chinese specific characteristics of sporadic Creutzfeldt-Jakob disease: a retrospective analysis of 57 cases.

Authors:  Wei Zhao; Jia-Tang Zhang; Xiao-Wei Xing; De-Hui Huang; Cheng-Lin Tian; Wei-Quan Jia; Xu-Sheng Huang; Wei-Ping Wu; Chuan-Qiang Pu; Sen-Yang Lang; Sheng-Yuan Yu
Journal:  PLoS One       Date:  2013-03-14       Impact factor: 3.240

4.  A case of Creutzfeldt-Jakob disease: diagnostic dilemmas of a rapidly fatal disease.

Authors:  Mirza M Baig; Martin Phillips
Journal:  Infect Dis Rep       Date:  2013-10-14
  4 in total

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