|
|||||
|
|
Distribution of prion protein in German patients with Creutzfeldt-Jakob disease is different from that in Japanese patients |
|
| Authors: | R. Doi-Yi T. Kitamoto K. Ogomori P. Mehraein J. Tateishi |
| Affiliation: | (1) Department of Neuropsychiatry, Kumamoto University Medical School, Honjo 1-1-1, 860 Kumamoto, Japan;(2) Department of Neuropathology, Neurological Institute, Faculty of Medicine, Kyushu University, Japan;(3) Department of Neuropsychiatry, School of Medicine, Kyushu University, Japan;(4) Institute of Neuropathology, University of Munich, Germany |
| Abstract: | We investigated the distribution of prion protein (PrP) in 14 German patients with sporadic Creutzfeldt-Jakob disease (CJD) and compared it with that observed in Japanese patients. Immunohistochemical study revealed diffuse gray matter stainings including synaptic structures in all cases. In addition, 4 patients showed plaque-type deposition which was very rarely observed among sporadic Japanese patients without known mutation of the PrP gene but with valine at codon 129. A higher incidence of PrP plaques in German sporadic CJD may be related to the racial difference in the PrP gene. |
| Keywords: | Creutzfeld-Jakob disease (CJD) Gerstmann-Strä ussler-Scheinker syndrome (GSS) Prion protein (PrP) Genotypes Phenotypes |
| 本文献已被 SpringerLink 等数据库收录！ | |