Huntington's disease

rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia
(Redirected from Huntington's Disease)

Huntington's disease is a genetic disorder caused by[2] mutation in a gene located on chromosome 4. It affects the brain and gets worse over time. This can lead to problems with moving, memory loss as well as thinking skills. Lastly, it also causes changes in behavior. Chorea is one of the main symptoms of Huntington's disease.

In 1872 George Huntington described the disorder in his first paper "On Chorea" at the age of 22.[1]
A microscope image of medium spiny neurons (yellow) with nuclear inclusions (orange): these are caused by the disease

On average, the disease leads to death about fifteen years after the first signs of the illness show. It is found in about 6 in 100,000 people. There is a 50% chance of inheriting this disease from the parents.[3] Medicine has been trying to find a cure for Huntington's disease for a long time.

History

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The disease is named after George Huntington. George Huntington specialized in medicine and psychology. In 1872, he was the first to describe the medical condition he was seeing in patients in a paper about science. In an 1908 review, an important scientist who also focused on medicine and psychology, William Osler, said about the paper: "In the history of medicine, there are few instances in which a disease has been more accurately, more graphically or more briefly described."

According to Huntington, the disease is characterized by three things: it is inherited; people who have it become cases for psychiatry (insanity and people who kill themselves); and it only occurs in adults. That was the medical understanding at that time. Of these, the last one is wrong: some children also show signs of the disease.[3]

Symptoms

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Symptoms of Huntington's disease usually begin between the ages of 35 and 44 years of age. They can, however, start in any age group from babies to old age.[4] Also, Huntington's disease kills the cells in the body and brain.

In fact, children with Huntington's disease are often much sicker. They get worse faster. Instead of having chorea, they usually have rigidity (or stiffness) of their muscles and it is painful. Seizures (uncontrollable movements in the body) are also a common sign in children.[4]

Treatment and care

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In 2015, there is still no treatment for the disease itself. There are medicines available to help with some of the symptoms. Tetrabenazine was approved in 2008 by the FDA. This medicine helps slow some of the restless movements of chorea.[5] Other medicines that can help with psychiatric symptoms and movements are benzodiazepines and anticonvulsants usually taken for seizures.[6]

Clinical trials

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Science Daily reported on May 6, 2019 that an international clinical trial has found a new drug is safe. It reported that the drug used by UBC researchers successfully lowers levels of Huntingtin protein.[7]

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References

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  1. Huntington G (1872). "On Chorea". Medical and Surgical Reporter of Philadelphia. 26 (15). The Hague: Nijhoff: 317–321. ISBN 9061860113. Retrieved 2009-04-01.
  2. "About Huntington's Disease and Related Disorders". www.hopkinsmedicine.org. Retrieved 2024-05-23.
  3. 3.0 3.1 Weiner, William J. 2016. Huntington's disease. World Book.
  4. 4.0 4.1 Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 218–28 [219]. doi:10.1016/S0140-6736(07)60111-1. PMID 17240289. S2CID 46151626.
  5. "FDA approves first drug for treatment of chorea in Huntington's disease". U.S. Food and Drug Administration. 15 August 2008. Archived from the original on 1 June 2012. Retrieved 10 August 2008.
  6. "Huntington Disease". Management: treatment of manifestations. The National Center for Biotechnology Information. 11 December 2014. Retrieved 4 February 2015.
  7. "Huntington drug successfully lowers levels of disease-causing protein, study shows".