On basic terms, nothing in your control can cause HD. You can not develop it because of foods you eat, or things you do. This particular disorder happens to not come into affect until ages 30-40 usually, even though the people that have it were born with it. Genetically speaking, on the short leg of the 4th chromosome, on the HTT gene, there is normally a sequence of repeating bases CAG. So it is normally CAGCAGCAGC... anywhere from 10-35 times, however, if it repeats 36-120 times, HD is developed. The more repeats, the earlier HD will come into your life. Some people with 100 repeats will start showing symptoms for HD at age 20, while others with 36-80 repeats won't start seeing the symptoms until ages 30-40.
HD results from genetically programmed degeneration of nerve cells, called neurons,* in certain areas of the brain. This degeneration causes uncontrolled movements, loss of intellectual faculties, and emotional disturbance. Specifically affected are cells of the basal ganglia, structures deep within the brain that have many important functions, including coordinating movement. Within the basal ganglia, HD especially targets neurons of the striatum, particularly those in the caudate nuclei and the pallidum. Also affected is the brain's outer surface, or cortex, which controls thought, perception, and memory. Hope this helps, friends!! :) :* <333
a dominant allele
Huntingtons disease is a genetic/inherited diesease. It is caused by a faulty allele (a dominant one), which can be inherited by parents. Spontanoius mutations may also occur which would cause the faulty gene and therefore huntingtons disorder.
The symptoms of Huntingtons Disease are, mental deterioration and uncontrollable movements; symptoms usually appear in middle ages.
No
Monosomy
No.
No.
One in ten thousand have Huntington's disease.
Huntingtons disease is inherited from your parents
Its Passed On From Your Parents Its Inherited
No.
medication and anti deprassants
Huntington's Chorea