A Guide to Undestanding Huntington’s Chorea

Huntington's chorea has been popular for over a century and was named by the general physician George Huntington based in New York in 1872. (Williams & Hopper, 2011). Huntington's disease is explained as a neurologic disease affecting human cognitive function, psychological function, and motor function. (Liew, 2013). It is inherently disintegrated and can not cure. (Aubeeluck & Wilson, 2008). In the United States alone, 1 in 10 people will affect. (Perrine Jr & Goodman, 1966).

Huntington's disease or Huntington's disease was named after Ohio State Doctor George Huntington in 1872. It is an inherited disorder characterized by abnormal body movements called chorea and memory loss. Choroid disease is an abnormal autonomous dyskinesia and is one of a group of nervous system disorders called dyskinesia caused by excessive activity of the neurotransmitter dopamine in the brain region controlling movement. Chorea is not repetitive or periodic, but is characterized by short irregular contractions that appear to flow from one muscle to the other. The incidence is 5 to 8 per 100,000 people. Understanding and treating Huntington's disease helps to save countless lives and individuals.

Huntington's chorea usually takes 10 to 25 years to kill someone. This is probably fatal. However, death is caused not by the disease itself but by complications caused by Huntington's disease. The average onset time of this disease is usually 30's and 40's. Approximately 10% of Huntington's dance cases occur in people under the age of 20 known as young Huntington's Disease. The symptoms of young Huntington's disease are quite different from the symptoms of adult born Huntington's disease. Adolescent individuals suffering from Huntington's disease often do not suffer from chorea and are often rigid or rigid (Wexler 157).

Huntington's disease is a fatal illness that almost always dies. More people should be aware of the risk of Huntington's disease and other genetic diseases. After allowing people to recognize the risk of hereditary diseases, new therapies and laws can be used to help people with these diseases. I hope that new treatments and understandings of these genetic diseases will be useful in treating current and future diseases.

Huntington's disease or Huntington's disease is a progressive neurodegenerative disease of the central nervous system inherited through an autosomal dominant gene. (Webster) It is caused by a mutation in the huntingtin protein in which the CAG repeat region is expanded. CAG is in charge of encoding glutamine. This mutation can cause many harmful effects and is eventually fatal. There is no known cure. - Huntington's disease is one of the most overwhelming diseases throughout the medical history. This is an inherited disorder caused by genetic changes that affect the brain's parents. It affects parts of the brain that control thought, emotion, and movement. This can cause uncontrollable movements in hands, feet, and face instability. What is affected by this disease is abnormal movement such as walking, talking, swallowing and so on.