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bovine spongiform encephalopathy |
Also found in: Encyclopedia, Wikipedia, Hutchinson | 0.04 sec. |
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encephalopathy /en·ceph·a·lop·a·thy/ (en-sef″ah-lop´ah-the) any degenerative brain disease. AIDS encephalopathy HIV e. anoxic encephalopathy hypoxic e. biliary encephalopathy , bilirubin encephalopathy kernicterus. bovine spongiform encephalopathy a transmissible spongiform encephalopathy of adult cattle, transmitted by feed containing protein in the form of meat and bone meal derived from infected animals. The etiologic agent is also the cause of new variant Creutzfeldt-Jakob disease. boxer's encephalopathy , boxer's traumatic encephalopathy slowing of mental function, confusion, and scattered memory loss due to continual head blows absorbed in the boxing ring. dialysis encephalopathy a degenerative disease of the brain associated with long-term use of hemodialysis, marked by speech disorders and constant myoclonic jerks, progressing to global dementia; it is due to high levels of aluminum in the dialysis fluid water or to aluminum-containing drugs used in treatment. hepatic encephalopathy a condition, usually occurring secondarily to advanced liver disease, marked by disturbances of consciousness that may progress to deep coma (hepatic coma), psychiatric changes of varying degree, flapping tremor, and fetor hepaticus. HIV encephalopathy , HIV-related encephalopathy AIDS encephalopathy; a progressive primary encephalopathy caused by human immunodeficiency virus type 1 infection, manifested by a variety of cognitive, motor, and behavioral abnormalities. hypoxic encephalopathy encephalopathy caused by hypoxia from decreased rate of blood flow or decreased oxygen in the blood; severe cases can cause permanent brain damage within five minutes. hypoxic-ischemic encephalopathy that resulting from fetal or perinatal asphyxia, characterized by feeding difficulties, lethargy, and convulsions. lead encephalopathy edema and central demyelination caused by excessive ingestion of lead compounds, particularly in young children. myoclonic encephalopathy of childhood a neurologic disorder of unknown etiology with onset between ages 1 and 3, characterized by myoclonus of trunk and limbs and by opsoclonus with ataxia of gait, and intention tremor; some cases have been associated with occult neuroblastoma. subacute spongiform encephalopathy , transmissible spongiform encephalopathy prion disease. Wernicke's encephalopathy an inflammatory hemorrhagic form due to thiamine deficiency, usually associated with chronic alcoholism, with paralysis of the eye muscles, diplopia, nystagmus, ataxia, and usually accompanying or followed by Korsakoff's syndrome.
Bovine spongiform encephalopathy A progressive, fatal disease of the nervous system of domestic animals. It is transmitted by eating infected food. Also known as Mad Cow disease. Mentioned in: Zoonosis bovine spongiform encephalopathy (BSE), an infection of cattle characterized by degenerative, clumsy, apprehensive behavior, and death. The BSE brain tissue is perforated and spongy in appearance. The disease was first observed in cattle by veterinarians in 1883. It has been associated with other spongiform encephalopathies such as scrapie in sheep and goats and Creutzfeldt-Jakob disease (CJD) in humans. In European "mad cow" disease, it is believed the disease was transmitted to cattle through livestock feed that contained remains of scrapie-infected sheep. The disease was then transmitted to humans who ate BSE-infected beef. bovine spongiform encephalopathy Bovine spongiform encephalitis, BSE, mad cow disease A disease of cattle, characterized by high-stepping or staggering gait, anxiety, ↑ sensitivity, and kicking while being milked, less commonly, frenzy,
aggression; BSE was first described in the UK in cows fed with sheep offal. See Prions. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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