| Huntington's chorea |
hereditary disease; develops in adulthood and ends in dementia
출처: wordnet.princeton.edu/perl/webwn
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| Huntington's chorea |
An autosomal dominant disease characterized by chronic progressive chorea and mental deterioration terminating in dementia; the age of onset is variable but usually in the fourth decade of life, with death within 15 years. [Dorland]
출처: www.antiquusmorbus.com/English/EnglishH.htm
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| Huntington's chorea |
A hereditary disease marked by degeneration of the basal ganglia in the cerebral cortex. Individuals develop progressive mental deterioration, ending in dementia, along with loss of the ability to control major muscle movements.
출처: www3.uta.edu/sswtech/sapvc/information/teens13_15/...
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| Huntington's chorea |
A fatal inherited disorder which has no cure. A progressive loss of mental functioning due to brain-cell death. Ten to twenty years after the onset of symptoms, victims will die; although they become little more than mindless organisms prior to the end. Science can identify some carriers of the Huntington's gene in utero.
출처: www.reasoned.org/glossary.htm
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| Huntington's chorea |
Autosomal Dominant. People die at 40 +... Jerky muscular motions
출처: www.mansfieldct.org/schools/mms/staff/hand/Genterm...
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