Creutzfeldt-Jakob disease

or Creutz·feldt-Ja·cob disease

[ kroits-felt yah-kawp ]

Phonetic (Standard)IPA

noun

Pathology.

a rare, usually fatal brain disorder thought to be caused by an infectious prion and characterized by progressive dementia, blindness, and involuntary movements.

Creutzfeldt-Jakob disease

/ ˈkrɔɪtsfɛlt ˈjɑːkɒp /

noun

pathol a fatal slow-developing disease that affects the central nervous system, characterized by mental deterioration and loss of coordination of the limbs. It is thought to be caused by an abnormal prion protein in the brain

Creutzfeldt-Jakob disease

A rare, usually fatal encephalopathy that occurs most often in middle age and is likely caused by a prion. It is characterized by progressive dementia and gradual loss of muscle control. The disease is named after its discoverers, German pathologist Hans Gerhard Creutzfeldt (1885–1964) and German neurologist Alfons Maria Jakob (1884–1931).

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Word History and Origins

Origin of Creutzfeldt-Jakob disease¹

1965–70; after German physicians Hans G. Creutzfeldt (1885–1964) and Alfons Jakob (1884–1931)

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Word History and Origins

Origin of Creutzfeldt-Jakob disease¹

C20: named after Hans G. Creutzfeldt (1885–1964) and Alfons Jakob (1884–1931), German physicians

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Example Sentences

Examples have not been reviewed.

The certificate also suggest that Creutzfeldt-Jakob disease may also have contributed to his death.

From

In people, the disease is fatal and called Creutzfeldt-Jakob disease.

From

Misfolding of the prion protein triggers prion diseases such as Creutzfeldt-Jakob disease.

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Anyone can donate their body with the exception of people with Creutzfeldt-Jakob disease, hepatitis B or C, HIV and active tuberculosis.

From

Hundreds of people fell ill, after eating contaminated meat, with the disorder caused in humans — named variant Creutzfeldt-Jakob disease — and many died.

From

Creuse crevalle

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