Illuminating Huntington’s disease
Huntington's disease (HD) is a progressive neurodegenerative disorder characterized by involuntary movements, cognitive decline, and emotional disturbances.1 Recent global prevalence data cites 4.88 per 100,000 persons and an incidence of 0.48 cases per 100,000 person-years.2
Overall, there has been a significant rise in cases, attributed to advancements in molecular genetic testing, earlier diagnosis, increased life expectancy among HD patients, and de novo mutations. In honor of Huntingdon’s Disease Awareness Month, we take a look at advances in pharmacological treatments for this condition.
A growing market
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