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860 Possible Causes for Prion Disease

  • Creutzfeldt Jakob Disease

    Classic CJD is a human prion disease. It is a neurodegenerative disorder with characteristic clinical and diagnostic features.[web.archive.org] Variant Creutzfeldt-Jakob disease (vCJD) is a prion disease that was first described in 1996 in the United Kingdom.[cdc.gov] CJD is classified as a transmissible spongiform encephalopathy (TSE) along with other prion diseases that occur in humans and animals.[cdc.gov]

  • Prion Disease

    prion disease.[ghr.nlm.nih.gov] Most patients with prion disease currently are diagnosed when they are about 2/3 of the way through their disease course (Geschwind et al., 2010a; Paterson et al., 2012b),[ncbi.nlm.nih.gov] This Review summarizes the evidence that immunization could slow disease progression or increase lifespan in animal models of prion diseases.[ncbi.nlm.nih.gov]

  • Insomnia

    The occurrence of sporadic prion disease among adolescents is extremely rare. A prion disease was confirmed in an adolescent with disease onset at 13 years of age.[ncbi.nlm.nih.gov] Fatal insomnia is a rare human prion disease characterised by sleep-wake disturbances, thalamic degeneration and deposition of type 2 disease-specific prion protein (PrP(Sc[ncbi.nlm.nih.gov] Sporadic fatal insomnia (sFI) and fatal familial insomnia (FFI) are rare human prion diseases.[ncbi.nlm.nih.gov]

  • Fatal Familial Insomnia

    To establish a variant of sporadic prion disease as the sporadic form of fatal familial insomnia (FFI).[ncbi.nlm.nih.gov] However in the case of inherited prion disease, the family history of neurological disease will be a very important pointer in the diagnosis.[alzheimer-europe.org] […] could be a prion disease.[doi.org]

  • Kuru

    BACKGROUND: Kuru provides the principal experience of epidemic human prion disease.[ncbi.nlm.nih.gov] PrP immunoblots of prion-diseased human brain.[ncbi.nlm.nih.gov] A number of genetic modifiers of prion disease have been mapped in mice ( 16, 17 ).[doi.org]

  • Familial Alzheimer-Like Prion Disease

    […] gene expression data for Familial Alzheimer-Like Prion Disease.[malacards.org] Suzuki , Koji Abe , Toru Iwaki , C-Terminal-Deleted Prion Protein Fragment Is a Major Accumulated Component of Systemic PrP Deposits in Hereditary Prion Disease With a 2-Bp[onlinelibrary.wiley.com] OBJECTIVE: To describe the Alzheimer disease (AD)-like clinical and pathological features, including marked neurofibrillary tangle (NFT) pathology, of a familial prion disease[ncbi.nlm.nih.gov]

  • Common Cold

    Prion diseases are a related group of rare, fatal brain diseases that affect animals and humans.[tools.wmflabs.org] PIDDs may be diagnosed in infancy, childhood, or adulthood, depending on disease severity.[tools.wmflabs.org]

  • Hypersensitivity

    Prion diseases are a related group of rare, fatal brain diseases that affect animals and humans.[niaid.nih.gov] PIDDs may be diagnosed in infancy, childhood, or adulthood, depending on disease severity.[niaid.nih.gov]

  • Sinusitis

    Prion diseases are a related group of rare, fatal brain diseases that affect animals and humans.[niaid.nih.gov] PIDDs may be diagnosed in infancy, childhood, or adulthood, depending on disease severity.[niaid.nih.gov]

  • Sexually Transmitted Disease

    Prion diseases are a related group of rare, fatal brain diseases that affect animals and humans.[niaid.nih.gov] PIDDs may be diagnosed in infancy, childhood, or adulthood, depending on disease severity.[niaid.nih.gov]

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