Hungtington’s Disease, also reffered to as “Hungtington’s Chorea”, is a neurodegenerative hereditary rare disease. Symptoms include motor, cognitive and psychiatric impairment resulting from neurodegeneration characteristic of the diseasing, ineluctably evolving to autonomy loss and death.
Hungtington’s Disease is caused by a single dominant defective gene on chromosome 4. An individual inheriting the gene from a parent will thus eventually develop the disease.
For the time being, no cure is available to teat Hungtington’s Disease or to slow down or stop cognitive, motor and psychiatric progression of the disease. Current therapies focus on helping patients managing symptoms.
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