WebBackground Huntington disease (HD) is a genetically inherited neurodegenerative disorder that classically involves a trinucleotide CAG repeat expansion on chromosome 4, with 36 repeats or greater being disease identifying. It generally presents between the age of 30 and 40 years old and is characterised by severe caudate/striatum degeneration with … WebDe ziekte van Huntington is een ongeneeslijke, erfelijke aandoening die bepaalde delen van de hersenen aantast. In het LUMC wordt u geholpen door artsen die jarenlange …
De ziekte van Huntington - Nederlands Herseninstituut - KNAW
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Wat is de ziekte van Huntington? - Atlant
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