Creutzfeldt-Jakob disease
noun
Forms Creutzfeldt–Jakob disease
- noun (pathology, neurology) A rare, progressive, fatal disease of the nervous system, characterized by dementia and loss of muscle control. It is a prion disease, apparently transmissible from animals to humans by eating infected tissue, as well as from tissue interchanges among humans (e.g. corneal transplants, blood transfusions).
Synonyms
Etymology
Named after German neurologists Hans Gerhard Creutzfeldt (1885–1964) and Alfons Maria Jakob (1884–1931).
Sources: Wiktionary · WordNet 3.0 — from the Wiktionary entry “Creutzfeldt-Jakob disease”, CC BY-SA 4.0. Details