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  2. Myoclonus - Wikipedia

    en.wikipedia.org/wiki/Myoclonus

    Most often, myoclonus is one of several signs in a wide variety of nervous system disorders [citation needed] such as multiple sclerosis, Parkinson's disease, dystonia, cerebral palsy, Alzheimer's disease, Gaucher's disease, subacute sclerosing panencephalitis, Creutzfeldt–Jakob disease (CJD), serotonin toxicity, some cases of Huntington's ...

  3. 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 ]

  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. 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.

  6. 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 ...

  7. Myoclonic triangle - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_triangle

    Lesions involving this circuit may produce palatal myoclonus, one of the few involuntary movements that do not disappear during sleep. [4] Palatal myoclonus may be seen as a component of the lateral medullary syndrome (a.k.a. Wallenberg Syndrome), if the infarction extends to involve the central tegmental tract.

  8. Palatal myoclonus - Wikipedia

    en.wikipedia.org/wiki/Palatal_myoclonus

    Palatal myoclonus is a rare condition in which there are rhythmic jerky movements or a rapid spasm of the palatal (roof of the mouth) muscles. Chronic clonus is often due to lesions of the central tegmental tract (which connects the red nucleus to the ipsilateral inferior olivary nucleus ).

  9. Unverricht–Lundborg disease - Wikipedia

    en.wikipedia.org/wiki/Unverricht–Lundborg_disease

    Unverricht–Lundborg disease was first known as one of two different diseases, depending on the location of the individual who had it: Baltic myoclonus or Mediterranean myoclonus. [7] The reason for the different names was partly regional but also because the prognosis of the disease was different for individuals with each due to the way that ...