Huntingtons chorea is a degenerative neurologic disorder that affects thousands of people across the globe. This disease is characterized by the impairment of physical and mental abilities. Symptoms usually begin to present surrounded by the ages of thirty to fifty-four but can also front as early as age four or as late as age eighty (Hubert Fernandez, MD. Chorea, Huntingtons disease). Typical symptoms include: depression, apathy, obsessive behaviour, inability to focus, think, recall and excite decisions, diminished coordination, involuntary movements, weight loss and inability to talk, crack and swallow (Huntington society of Canada, What is Huntington Disease?).
Huntingtons chorea is a hereditary disease meaning that it is passed on through genetic science from pargonnts to children. However, roughly one to three percent of reported cases bemuse no prior family history. Theses cases are thought to be caused by a gene mutation during meiosis. The genetic defect that causes Huntingtons disease is located on chromosome four denoting that it is an autosomal disorder. The Huntingtons gene is dominant which means that any offspring of a parent with Huntingtons has a fifty percent scene of inheriting the disease (MedicineNet.com, Huntingtons Disease).
At this time Huntingtons chorea is a terminal illness with no cure. However, on that point are various medications doctors may prescribe to help alleviate the symptoms. Also, there is a great extent of research being through to help increase our understanding of the disease. Gene therapy, for instance, is a shiny new word for hereditary diseases. This therapy involves inserting a new substitute(a) form of the gene into a cell in hopes of permutation the defective gene. Although gene therapy has yet to be an approved treatment for Huntingtons it has been successful in curing certain different diseases (Healthtree, Gene Therapy for Huntingtons).
Research has also lead scientists to discover that...If you privation to get a full essay, order it on our website: Orderessay
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