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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. Transmissible spongiform encephalopathy - Wikipedia

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

    Prion disease: Micrograph showing spongiform degeneration (vacuoles that appear as holes in tissue sections) in the cerebral cortex of a patient who had died of Creutzfeldt–Jakob disease. H&E stain, scale bar = 30 microns (0.03 mm). Specialty: Infectious diseases Symptoms: Dementia, seizures, tremors, insomnia, psychosis, delirium, confusion ...

  4. List of zoonotic diseases - Wikipedia

    en.wikipedia.org/wiki/List_of_zoonotic_diseases

    Creutzfeldt-Jacob disease: PrP vCJD: cattle eating meat from animals with Bovine spongiform encephalopathy (BSE) 1996–2001: United Kingdom. Crimean–Congo hemorrhagic fever: Crimean-Congo hemorrhagic fever orthonairovirus: cattle, goats, sheep, birds, multimammate rats, hares tick bite, contact with bodily fluids Cryptococcosis: Cryptococcus ...

  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. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.

  7. Gerstmann–Sträussler–Scheinker syndrome - Wikipedia

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

    GSS is a disease that progresses slowly, lasting roughly 2–10 years, with an average of approximately five years. [8] [1] Symptoms as clumsiness and unsteadiness when walking at the beginning of the illness. Muscle jerking (myoclonus) is much less common than in Creutzfeldt-Jakob disease.

  8. Adrenoleukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Adrenoleukodystrophy

    One of the difficulties with ALD as a disease included in universal newborn screening is the difficulty in predicting the eventual phenotype that an individual will express. The accepted treatment for affected boys presenting with the cerebral childhood form of the disease is a bone marrow transplant, a procedure which carries significant risks.

  9. List of notifiable diseases - Wikipedia

    en.wikipedia.org/wiki/List_of_notifiable_diseases

    Disease Australia [1] Hong Kong [2] India [3] Malaysia [4] United Kingdom [5] United States [6] Amoebic dysentery: Yes Yes Babesiosis: Yes Cancer: Yes Coccidioidomycosis: Yes Creutzfeldt–Jakob disease (CJD) Yes Yes variant Creutzfeldt–Jakob disease (vCJD) Yes Cryptosporidiosis: Yes Yes Cyclosporiasis: Yes Dysentery: Yes Yes Fever syndromes ...