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Huntington’s disease is a progressive, neurodegenerative disorder that’s caused by a genetic mutation in the gene coding for the huntingtin protein, inherited in an autosomal dominant pattern.
HD is a hereditary disorder of the central nervous system. It used to be known as Huntington's chorea. Huntington's disease usually develops in adulthood and can cause a very wide range of symptoms (Huntingdon's Disease Association, 2008).
Huntington's disease part 1: what is it? - University of the Sunshine ...
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A recent Huntington’s disease genome-wide association study found rs557874766, an imputed single nucleotide polymorphism located within a polymorphic 9 bp tandem repeat in MSH3/DHFR, as the variant most significantly associated with progression in Huntington’s disease.
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