mlevine1 Posted October 8, 2015 Share Posted October 8, 2015 Huntington’s disease (HD) is an inheritable neurological disorder caused by a triplet repeat (CAG) expansion in the huntingtin (HTT) gene located in the short arm of chromosome four. Symptoms include uncontrollable dance-like movements (chorea), cognitive deficits, and psychiatric disturbances. Some of the early, or prodromic, symptoms include an inability to shift attention and other behavioral inflexibilities.Link back to full article Link to comment Share on other sites More sharing options...
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