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  2. List of human disease case fatality rates - Wikipedia

    en.wikipedia.org/wiki/List_of_human_disease_case...

    Human infectious diseases may be characterized by their case fatality rate (CFR), the proportion of people diagnosed with a disease who die from it (cf. mortality rate).It should not be confused with the infection fatality rate (IFR), the estimated proportion of people infected by a disease-causing agent, including asymptomatic and undiagnosed infections, who die from the disease.

  3. Transmissible spongiform encephalopathy - Wikipedia

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

    Transmissible spongiform encephalopathies (TSEs), also known as prion diseases, [1] are a group of progressive, incurable, and fatal conditions that are associated with the prion hypothesis and affect the brain and nervous system of many animals, including humans, cattle, and sheep.

  4. Transmissible mink encephalopathy - Wikipedia

    en.wikipedia.org/wiki/Transmissible_mink...

    Transmissible mink encephalopathy was first noticed in 1947 on a mink farm in the United States, in Brown County, Wisconsin, but the disease was not reported in the scientific literature until 1965. Upon reviewing prior TME outbreaks in the U.S. and Canada, in all four cases which were not linked to a commercial feed plant and in which records ...

  5. Prion - Wikipedia

    en.wikipedia.org/wiki/Prion

    All known prion diseases are untreatable and fatal. [9] [83] [84] Until 2015 all known mammalian prion diseases were considered to be caused by the prion protein, PrP; in 2015 multiple system atrophy was found to be transmissible and was hypothesized to be caused by a new prion, the misfolded form of a protein called alpha-synuclein. [10]

  6. 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 ]

  7. Gerstmann–Sträussler–Scheinker syndrome - Wikipedia

    en.wikipedia.org/wiki/Gerstmann–Sträussler...

    Gerstmann–Sträussler–Scheinker syndrome (GSS) is an extremely rare, always fatal (due to it being caused by prions) neurodegenerative disease that affects patients from 20 to 60 years in age. It is exclusively heritable, and is found in only a few families all over the world. [ 1 ]

  8. Template:Prion diseases - Wikipedia

    en.wikipedia.org/wiki/Template:Prion_diseases

    To change this template's initial visibility, the |state= parameter may be used: {{Prion diseases | state = collapsed}} will show the template collapsed, i.e. hidden apart from its title bar. {{Prion diseases | state = expanded}} will show the template expanded, i.e. fully visible. for test edits on this template, go here

  9. Case fatality rate - Wikipedia

    en.wikipedia.org/wiki/Case_fatality_rate

    In epidemiology, case fatality rate (CFR) – or sometimes more accurately case-fatality risk – is the proportion of people who have been diagnosed with a certain disease and end up dying of it. Unlike a disease's mortality rate , the CFR does not take into account the time period between disease onset and death.