In Huntington's disease, the primary target of damage is the basal ganglia, particularly the striatum, which includes the caudate nucleus and putamen. This neurodegenerative disorder is characterized by the progressive loss of neurons in these areas, leading to motor dysfunction, cognitive decline, and psychiatric symptoms. The underlying cause is a mutation in the HTT gene, which results in the production of an abnormal protein that ultimately causes cellular toxicity and neuronal death.
The symptoms of Huntingtons Disease are, mental deterioration and uncontrollable movements; symptoms usually appear in middle ages.
Monosomy
No.
No.
No
One in ten thousand have Huntington's disease.
Its Passed On From Your Parents Its Inherited
medication and anti deprassants
No.
Huntingtons disease is inherited from your parents
Huntington's Chorea
HD is a genetic disease, and currently cannot be prevented.