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  2. Creutzfeldt–Jakob disease - Wikipedia

    en.wikipedia.org/wiki/Creutzfeldt–Jakob_disease

    Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is a fatal neurodegenerative disease. [ 4 ] [ 1 ] Early symptoms include memory problems, behavioral changes, poor coordination, and visual disturbances. [ 4 ]

  3. Fatal insomnia - Wikipedia

    en.wikipedia.org/wiki/Fatal_insomnia

    Fatal insomnia is an extremely rare neurodegenerative prion disease that results in trouble sleeping as its hallmark symptom. [2] The majority of cases are familial (fatal familial insomnia [FFI]), stemming from a mutation in the PRNP gene, with the remainder of cases occurring sporadically (sporadic fatal insomnia [sFI]).

  4. Transmissible spongiform encephalopathy - Wikipedia

    en.wikipedia.org/wiki/Transmissible_spongiform...

    For example, Creutzfeldt–Jakob disease has been transmitted to patients taking injections of growth hormone harvested from human pituitary glands, from cadaver dura allografts and from instruments used for brain surgery (Brown, 2000) (prions can survive the "autoclave" sterilization process used for most surgical instruments).

  5. Variant Creutzfeldt–Jakob disease - Wikipedia

    en.wikipedia.org/wiki/Variant_Creutzfeldt–Jakob...

    vCJD is a separate condition from classic Creutzfeldt–Jakob disease (though both are caused by PrP prions). [9] Both classic and variant CJD are subtypes of Creutzfeldt–Jakob disease. There are three main categories of CJD disease: sporadic CJD, hereditary CJD, and acquired CJD, with variant CJD being in the acquired group along with ...

  6. Creutzfeldt-Jakob Disease Surveillance System - Wikipedia

    en.wikipedia.org/wiki/Creutzfeldt-Jakob_Disease...

    The Creutzfeldt-Jakob Disease Surveillance System (CJDSS) is a unit of the Public Health Agency of Canada. It studies the various variants of Creutzfeldt-Jakob Disease , and at least as of 2017, assisted "with DNA sequencing , autopsy and case confirmation". [ 1 ]

  7. United Kingdom BSE outbreak - Wikipedia

    en.wikipedia.org/wiki/United_Kingdom_BSE_outbreak

    The United Kingdom was afflicted with an outbreak of bovine spongiform encephalopathy (BSE, also known as "mad cow disease"), and its human equivalent variant Creutzfeldt–Jakob disease (vCJD), in the 1980s and 1990s. Over four million head of cattle were slaughtered in an effort to contain the outbreak, and 178 people died after contracting ...

  8. Abbrev. [1]Meaning [1] Latin (or Neo-Latin) origin [1]; a.c. before meals: ante cibum a.d., ad, AD right ear auris dextra a.m., am, AM morning: ante meridiem: nocte ...

  9. New Brunswick neurological syndrome of unknown cause

    en.wikipedia.org/wiki/New_Brunswick_neurological...

    In 2013, Moncton, New Brunswick-based neurologist, Alier Marrero of the Dr. Georges-L.-Dumont University Hospital Centre had requested CJDSS assistance in running tests on a suspected case of Creutzfeldt-Jakob disease (CJD) – an incurable, fatal disease. The results were negative.