No, it is a dominant gene
The symptoms of Huntingtons Disease are, mental deterioration and uncontrollable movements; symptoms usually appear in middle ages.
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.
Monosomy
No.
No.
No
No, the traits for Huntington's disease are not carried on more than one chromosome. The condition is caused by a mutation in the HTT gene, which is located on chromosome 4. This genetic mutation leads to the production of an abnormal version of the huntingtin protein, ultimately causing the symptoms associated with the disease.
Hungtington's disease is a dominant mutation in the gene that codes for the protein 'Huntington' It only affects a single gene, the remainder of the chromosome is unaffected and therefore it is not a chromosomal abnormality
One in ten thousand have Huntington's disease.
Its Passed On From Your Parents Its Inherited
medication and anti deprassants
No.