Category: Neurology / Neurodegenerative Disorders
Huntington's disease is a progressive, inherited neurodegenerative disorder characterized by uncontrolled movements (chorea), cognitive decline, and psychiatric problems, caused by an expansion of a CAG trinucleotide repeat in the HTT gene.
Approximately 2.7 per 100,000 people of European descent; less common in other populations (Source: Huntington's Disease Society of America)
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