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chorea

   Also found in: Dictionary/thesaurus, Medical, Wikipedia, Hutchinson 0.04 sec.
chorea (kərē`ə, kō–) or St. Vitus's dance, acute disturbance of the central nervous system nervous system, network of specialized tissue that controls actions and reactions of the body and its adjustment to the environment. Virtually all members of the animal kingdom have at least a rudimentary nervous system.
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 characterized by involuntary muscular movements of the face and extremities. The disease, known also as Sydenham's chorea (not to be confused with Huntington's disease Huntington's disease, hereditary, acute disturbance of the central nervous system usually beginning in middle age and characterized by involuntary muscular movements and progressive intellectual deterioration; formerly called Huntington's chorea.
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, a hereditary disease of adults that is sometimes called Huntington's chorea), is usually, but not always, a complication of rheumatic fever rheumatic fever (r
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. Sydenham's chorea, a disease of children, especially females, usually appears between the ages of 7 and 14. Facial grimacing and jerking movements persist for 6 to 10 weeks and sometimes recur after months or even years. Eventually the symptoms disappear. Although there is no specific treatment, sedatives and tranquilizers are helpful in suppressing the involuntary movements. Technically, it is sometimes called chorea minor or juvenile chorea to distinguish it from several less common choreas, chorea also being a general term for continuous, involuntary jerking movements.

chorea

Neurological disorder causing irregular, involuntary, purposeless movements. It is believed to be caused by degeneration of the basal ganglia in the cerebral cortex. Sydenham chorea (St. Vitus dance) is usually associated with rheumatic fever. It usually occurs between ages 5 and 15, more often in girls. Typical jerking movements, mostly in the extremities and face, may affect speech and swallowing and range from mild to incapacitating; attacks last several weeks and recur frequently. Senile chorea, a progressive disease resembling Sydenham chorea, usually occurs late in life. Huntington chorea is rare, hereditary, and fatal. It usually begins between ages 35 and 50 and progresses to random, often violent, and eventually totally incapacitating spasms, absent only during sleep. Mental deterioration begins later, and death occurs in 10–20 years. There is no effective therapy. Children of those afflicted have a 50% chance of developing the illness.


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often are referred to as chorea (dance-like or writhing in nature) and occur fewer than two times per second.
Other neurologic signs, such as chorea, dystonia, and myoclonus, commonly develop late in the course of vCJD.
Several teams are looking into the misfolding of proteins, which scientists theorize to be the problem underlying brain illnesses, including Alzheimer's disease and Huntington's chorea.
 
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