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  2. Huntington's disease - Wikipedia

    en.wikipedia.org/wiki/Huntington's_disease

    Huntington's disease (HD), also known as Huntington's chorea, is an incurable neurodegenerative disease [7] that is mostly inherited. [8] The earliest symptoms are often subtle problems with mood or mental/psychiatric abilities. [9][1] A general lack of coordination and an unsteady gait often follow. [2] It is also a basal ganglia disease ...

  3. Hyperkinesia - Wikipedia

    en.wikipedia.org/wiki/Hyperkinesia

    Hyperkinesia, more specifically chorea, is the hallmark symptom of Huntington's disease, formerly referred to as Huntington's chorea. Appropriately, chorea is derived from the Greek word, khoros, meaning "dance." The extent of the hyperkinesia exhibited in the disease can vary from solely the little finger to the entire body, resembling ...

  4. Chorea - Wikipedia

    en.wikipedia.org/wiki/Chorea

    Treatment; Huntington's-related: A common treatment is dopaminergic antagonists, although treatment is largely supportive. Tetrabenazine is the only FDA approved drug for the treatment of Huntington's disease-related chorea. Sydenham's chorea: Haloperidol, carbamazepine and valproic acid.

  5. Tetrabenazine - Wikipedia

    en.wikipedia.org/wiki/Tetrabenazine

    Tetrabenazine is a drug for the symptomatic treatment of hyperkinetic movement disorders. It is sold under the brand names Nitoman and Xenazine among others. On August 15, 2008, the U.S. Food and Drug Administration approved the use of tetrabenazine to treat chorea associated with Huntington's disease. Although other drugs had been used " off ...

  6. Basal ganglia disease - Wikipedia

    en.wikipedia.org/wiki/Basal_ganglia_disease

    Sydenham's chorea is a disorder characterized by rapid, uncoordinated jerking movements primarily affecting the face, hands and feet. [13] It is a result of an autoimmune response that occurs following infection by group A β-hemolytic streptococci (GABHS) [ 14 ] that destroys cells in the corpus striatum of the basal ganglia .

  7. Deutetrabenazine - Wikipedia

    en.wikipedia.org/wiki/Deutetrabenazine

    323.462 g·mol −1. Deutetrabenazine (trade name Austedo) is a vesicular monoamine transporter 2 inhibitor which is used for the treatment of chorea associated with Huntington's disease and tardive dyskinesia. Chemically, deutetrabenazine is an isotopic isomer of tetrabenazine in which six hydrogen atoms have been replaced by deuterium atoms.

  8. George Huntington - Wikipedia

    en.wikipedia.org/wiki/George_Huntington

    George Huntington (April 9, 1850 – March 3, 1916) was an American physician who contributed a classic clinical description of the disease that bears his name— Huntington's disease. [1] Huntington described this condition in the first of only two scientific papers he ever wrote. He wrote this paper when he was 22, a year after receiving his ...

  9. Tardive dyskinesia - Wikipedia

    en.wikipedia.org/wiki/Tardive_dyskinesia

    Tardive dyskinesia is believed to involve the neurotransmitter dopamine. Tardive dyskinesia (TD) is a disorder that results in involuntary repetitive body movements, which may include grimacing, sticking out the tongue or smacking the lips. [1] Additionally, there may be chorea or athetosis. [1] In about 20% of people with TD, the disorder ...