creutzfeldt-jakob disease

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creutzfeldt-jakob disease

Creutzfeldt-Jakob hastalığı

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Creutzfeldt-Jakob disease

A rare, progressive, currently fatal disease of the nervous system, characterized by dementia and loss of muscle control. A prion disease, apparently transmissible from animals to humans by eating infected tissue, as well as from tissue interchanges among humans (corneal transplants, blood transfusions)

Creutzfeldt-Jakob disease

CJD a very serious disease that kills people and that may be caused by eating beef that is infected with BSE. or CJD Rare fatal disease of the central nervous system. It destroys brain tissue, making it spongy and causing progressive loss of mental functioning and motor control. The disease commonly arises in adults between the ages of 40 and

Creutzfeldt-Jakob disease

CJD, rare degenerative brain disease named after Hans G. Creutsfeldt and Alfons Jakob (disease is characterized by memory loss, jerky movements, stiff posture and seizures caused by a rapid loss of cerebral cells)

Creutzfeldt-Jakob disease

Patients usually die within a year. There is no known cure. The disease is caused by a prion that builds up in neurons. Inherited or random mutation accounts for 99% of cases; the rest come from prion exposure during medical procedures and possibly from eating the meat of cattle with mad cow disease

creutzfeldt-jakob disease

rare (usually fatal) brain disease (usually in middle age) caused by an unidentified slow virus; characterized by progressive dementia and gradual loss of muscle control

Creutzfeldt-Jakob disease.

CJD

Creutzfeldt Jakob Disease

cjd

Heceleme

creutzfeldt-jakob dis-ease

Etimoloji

() Named after Hans Gerhard Creutzfeldt and Alfons Maria Jakob.