Problem

Huntington's disease

Other Names:
Huntington's chorea
Nature:

Huntington's disease (HD) is a degenerative brain disorder for which at present there is no cure. Typically, the disease begins in midlife, between the ages of 30 and 45, although onset may occur at any age. Early symptoms can be mild enough to go unnoticed at first and may include depression, mood swings, forgetfulness, clumsiness, twitching, and lack of coordination. Advanced symptoms are: personality changes, unsteady gait, involuntary movements; slurred speech; impaired judgement; difficulty in swallowing; and intoxicated appearance. As the disease progresses, usually over a 10 to 15 year period, the severity of symptoms increases. Concentration and short-term memory are diminished and involuntary movements become more pronounced. Walking and everyday activities become difficult, and speech and swallowing abilities deteriorate.

Incidence:

An estimated 30,000 Americans have Huntington's disease. Males and females are affected equally and HD crosses all racial and ethnic boundaries. A further 150,000 have a 50-50 chance of inheriting the disease from an affected parent and are said to be 'at risk.' Those who do not inherit HD cannot pass it on to their children and the chain of inheritance is broken.

Values:
Disease
Problem Type:
G: Very specific problems
Related UN Sustainable Development Goals:
GOAL 3: Good Health and Well-being
Date of last update
15.07.2019 – 16:37 CEST