A Creutzfeldt-Jakob-betegségröl.

Translated title of the contribution: Creutzfeldt-Jakob disease

Research output: Contribution to journalArticle

Abstract

A most common form of human prion disease, also known as non-conventional slow virus diseases; Creutzfeldt-Jakob's disease is described in detail. The available data on the pathogenesis of the illness have recently changed and constitute a most exciting article of contemporary medicine. 109 cases are introduced that have been verified neuropathologically in Hungary until now; their summed up clinical data, the pathological findings and their epidemiological characteristics are discussed. It must be emphasized that the diagnosis of the illness cannot be inevitably confirmed clinically. Transplantation of organs or tissues of all deceased, who suffered of an illness with dementia, should be strictly avoided accordingly.

Original languageHungarian
Pages (from-to)2895-2901
Number of pages7
JournalOrvosi hetilap
Volume137
Issue number52
Publication statusPublished - Dec 29 1996

    Fingerprint

ASJC Scopus subject areas

  • Medicine(all)

Cite this