Huntington's disease


(chorea) A rare hereditary and progressive degenerative disease of the central nervous system transmitted as an autosomal dominant trait.  Onset is typically in middle adult life with involuntary movements of the face, hands, and shoulders.  These movements become more pronounced and often result in a massive jerkiness of the limbs, facial muscles, and diaphragm.  Progressive dementia typically parallels the movement disorder and the person is incapable of doing anything.  Psychosis may develop, most commonly depression that varies in degree (ill-sustained).

Source: Edgerton, Jane E. 1994. American Psychiatric Glossary, 7th Edition. Washington, DC: American Psychiatric Press











   

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