
Huntington's Disease (HD), also known as Huntington Disease or Huntington's Chorea, is an inherited neurological disorder.
It is usually characterised by involuntary movement and intellectual, emotional and behavioural problems.
In most cases HD is a "late" onset disease and symptoms generally appear when a person reaches their mid thirties or forties. In rare cases HD may develop in childhood or as late as seventy years of age.
Treatment of HD and research into its causes has greatly improved in recent years. The HD gene was isolated in 1993 but there is still no cure for the disease.
[This page is based on the Association's publication Huntington's Disease. Originally written by Dennis H. Phillips, Ph.D. and first published in 1981, it has been frequently revised and republished since then. The current edition was published in 2001. (Australian Huntington's Disease Association (NSW) Inc. Huntington's Disease West Ryde, 2001.)]|
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