Literature DB >> 8768606

[Creutzfeldt-Jakob disease. Clinical, electrophysiological and histopathological correlations].

M Martínez Barros1, J Ramos Peek, R Vega, A Escobar.   

Abstract

Creutzfeldt-Jakob disease (CJD) is one of a small group of the so-called spongiform encephalopathies. It is a rare transmissible disorder which is characterized by progressive and irreversible neurological damage. There are few reports where clinical manifestations are correlated with neurophysiologic and histopathologic findings. The present paper includes three cases of CJD where alterations in evoked potentials and brain mapping studies gave valuable information, especially in those where the clinical picture and the electroencephalogram were non-specific, we conclude that these alterations suggest that the classic histopathological changes in C-J disease involves both cortical and subcortical structures.

Entities:  

Mesh:

Year:  1995        PMID: 8768606

Source DB:  PubMed          Journal:  Gac Med Mex        ISSN: 0016-3813            Impact factor:   0.302


  2 in total

1.  Can prion disease suspicion be supported earlier? Clinical, radiological and laboratory findings in a series of cases.

Authors:  Alejandra González-Duarte; Zaira Medina; Rainier Rodriguez Balaguer; Jesus Higuera Calleja
Journal:  Prion       Date:  2011-07-01       Impact factor: 3.931

2.  Abnormalities in Brainstem Auditory Evoked Potentials in Sheep with Transmissible Spongiform Encephalopathies and Lack of a Clear Pathological Relationship.

Authors:  Timm Konold; Laura J Phelan; Saira Cawthraw; Marion M Simmons; Melanie J Chaplin; Lorenzo González
Journal:  Front Vet Sci       Date:  2016-08-02
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.