Huntington's disease is considered a rare genetic disorder, affecting approximately 3 to 7 per 100,000 people in the general population. It is caused by a mutation in the HTT gene and typically manifests in mid-adulthood, leading to progressive motor, cognitive, and psychiatric symptoms. While the disease is relatively rare, its impact can be significant for affected individuals and their families.
Get Lost - Huntingtons album - was created in 1999-01.
It can be, especially for the family.
The symptoms of Huntingtons Disease are, mental deterioration and uncontrollable movements; symptoms usually appear in middle ages.
Yes. The involuntary movements of Huntington's were thought to resemble a kind of dance (chorea - like choreograph).
Monosomy
No.
No
No, it is autosomal dominant.
No.
Around 1 in 10,000 people are estimated to develop Huntington's disease, a rare genetic disorder. It is caused by a mutation in the HTT gene on chromosome 4.
Its Passed On From Your Parents Its Inherited
medication and anti deprassants