Creutzfeldt-Jakob disease

Creutzfeldt-Jakob disease
also Creutzfeld-Jakob disease noun Etymology: Hans G. Creutzfeldt died 1964 German psychiatrist and Alfons M. Jakob died 1931 German psychiatrist Date: 1963 a rare progressive fatal encephalopathy caused by a prion and marked by development of porous brain tissue, premature dementia in middle age, and gradual loss of muscular coordination

New Collegiate Dictionary. 2001.

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  • Creutzfeldt–Jakob disease — Classification and external resources Tonsil biopsy in variant CJD. Prion Protein immunostaining. ICD 10 A …   Wikipedia

  • Creutzfeldt-Jakob disease — ► NOUN ▪ a fatal degenerative disease affecting nerve cells in the brain. ● new variant Creutzfeldt Jakob disease Cf. ↑new variant Creutzfeldt Jakob disease ORIGIN named after the German neurologists H. G. Creutzfeldt and A. Jakob, who first… …   English terms dictionary

  • Creutzfeldt-Jakob disease — [kroits΄felt yä′kōb, kroits΄feld yä′kôp] n. an incurable degenerative disease of the nervous system thought to be caused by an unusual virus that incubates in the body for many years before symptoms appear …   English World dictionary

  • Creutzfeldt-Jakob disease — Infobox Disease Name = Creutzfeldt Jakob disease Caption = DiseasesDB = 3166 ICD10 = ICD10|A|81|0|a|80, ICD10|F|02|1|f|00 ICD9 = ICD9|046.1 ICDO = OMIM = 123400 MedlinePlus = eMedicineSubj = neuro eMedicineTopic = 725 MeshID = D007562 Creutzfeldt …   Wikipedia

  • Creutzfeldt-Jakob disease — /kroyts felt yah kawp/, Pathol. a rare, usually fatal brain disorder caused by an unidentified pathogen and characterized by progressive dementia, blindness, and involuntary movements. Also, Creutzfeldt Jacob disease. Also called Jakob… …   Universalium

  • Creutzfeldt-Jakob disease — noun 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 • Syn: ↑CJD, ↑Jakob Creutzfeldt disease • Hypernyms: ↑brain disorder,… …   Useful english dictionary

  • Creutzfeldt-Jakob disease — Creutz·feldt Ja·kob disease also Creutz·feld Ja·kob disease .krȯits .felt .yä (.)kōb n a rare progressive fatal spongiform encephalopathy now usu. considered to be caused by a prion and marked by the development of porous brain tissue, premature …   Medical dictionary

  • Creutzfeldt-Jakob disease — CJD a rapidly progressive rare neurological disease, a form of human spongiform encephalopathy in which dementia progresses to death after a period of 3–12 months. There is no effective treatment. The causative agent is an abnormal prion protein… …   The new mediacal dictionary

  • Creutzfeldt–Jakob disease — [ˌkrɔɪtsfɛlt jakɒb] noun a fatal degenerative disease affecting nerve cells in the brain, believed to be caused by a prion. Phrases new variant Creutzfeldt–Jakob disease a form of the disease characterized by an early age of onset and possibly… …   English new terms dictionary

  • Creutzfeldt-Jakob disease — Creutz·feldt Ja·kob dis·ease || ‚krɔɪtsfelt jækÉ’b 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… …   English contemporary dictionary

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