Creutzfeldt-Jakob disease (CJD) is the most important human transmissible s
pongiform encephalopathy (prion disease), recognised in sporadic, genetic b
ut also iatrogenic forms. The identification of 8 health care workers in a
group of 114 definitive CJD patients in Slovakia suggested the possibility
of professionaly acquired CJD and induced the investigation of potential en
do- and exogenous risk factors. In CJD-affected health professionals specia
l attention was paid to a detailed occupational history, including a possib
le professional contact with CJD patient and to the findings characteristic
for iatrogenic CJD: early cerebellar symptomatology, long duration of the
disease, absence of typical EEG finding and homozygosity of PRNP gene at co
don 129. Analysis of epidemiological, clinical and molecular biological dat
a in investigated group of CJD-affected health professionals gave no eviden
ce of an occupational risk for CJD.