Compare And Contrast The Battle Between Disease And Technology

Huntington’s Disease is a brain disorder affecting movement, cognition, and emotions (Schoenstadt). It is a genetic disorder generally affecting people in their middle 30s and 40s (Sheth). Worldwide, Huntington’s disease (affects between 3-7 per 100,000 people of European ancestry (Schoenstadt). In the United States alone, 1 in every 30,000 people has Huntington’s disease (Genetic Learning Center). Huntington’s Disease is a multi-faceted disease, with a complex inheritance pattern and a wide range of symptoms. There is also much research being done in the field of Huntington’s disease, because as of 2012, this disease is untreatable. THESIS.

The genetic disorder is caused by a mutation in the DNA segment CAG found in chromosome 4 which results nerve cell death. Phenotypic characteristics include gradual motor dysfunction, psychological issues that correlate to degeneration of metal health, and cognitive degeneration. Studies on transgenic mice have allowed a better understanding of the proteins that relate to Huntington’s

Huntington's Disease is a genetic autosomal disorder which effects the brain. It affects about 1 in 20,000 individuals. The symptoms of the disease do not start to occur until after or around 40 years of age. With the onset of the disease the patient starts to gradually deteriorate intellectually, this deterioration also causes involuntary movements. Scientists have only recently found the section of the gene which causes Huntington's disease, and this is allowed them to devise pre-symptomatic tests. However, a cure for the disease is yet to be found.

Huntington's Disease (HD) is an autosomal dominant, progressive, neurodegenerative disorder (Walker, 2007 and Harmon, 2007). The gene that causes the disease is located on the fourth chromosome and causes an abnormal number of repeats in the patient's genetic code (Harmon, 2007). Huntington's Disease can have devastating effects on patients' quality of life. The first symptoms of HD generally start between the ages of 30 and 45 and patients are typically asymptomatic prior to this time (Terrenoire, 1992 and Walker, 2007). However, the disease progresses with subtle changes in motor control, personality, and cognition. Patients eventually develop distinct

Huntington's Disease (HD) is a disability that will continue to get worse and worse over time. The lifespan for someone living with HD is 10 to 25 years after they are diagnosed and showing symptoms, which is usually around the ages of 30 to 50 ("What Is Huntington's Disease," 2017). These symptoms begin at different times and depend on the individual. Overtime, the person affected will begin to lose their ability to walk, talk, and eat over the course of these 10 to 25 years resulting in the need for 24 hour care.

Huntington's disease is an autosomal dominant disorder, which is found on the # 4 chromosome. George Huntington discovered it in 1872. It mainly has an effect on the nervous system. There are around 210,000 bases between D4S180 and D4S127. The disease itself is found in 2% of people in their childhood, and in 5% of the people they were older then 60. (Miller p 16) In the majority of the affected people the disease is detected between the ages of 35-45. In males the disease begins around the time of their childhood. However, in females it begins later in life. This severe symptom has a tendency for the condition to worsen as it is passed on from generation to generation. Huntington’s disease is paternally

Huntington's disease is an inherited genetic disease which can’t be cured. (Staff, M. C , 2014) Huntington's disease is caused by an inherited defect in a single gene. A parent with a defective Huntington gene could pass along the defective copy of the gene or the healthy copy. Each child in the family, therefore, has a 50 percent chance of inheriting the gene that causes the genetic disorder.Huntington’s disease has a broad impact on a patients’ functional abilities and thinking and psychiatric disorders. They get involuntary jerking or writing movements (chorea), have difficulty organizing tasks and learning new things. (Staff, M. C , 2014) Patients act like the girl in Andersen’s fairy tales

The next disease being discussed, Huntington’s Disease, is a hereditary progressive neurodegenerative disorder that can affect the psyche, emotions, and behavior. However, it is most commonly known for the loss of cognitive functioning as well as motor disturbances (Leffler, 2011). Usually the initial signs of Huntington’s Disease starts with jerky movements that can affect various parts of the body (face, arms, legs, etc.) as well as the gradual beginnings of dementia; the memory is usually impaired. There also may be disorientation, or disillusioned ideas of time, place or identity, as well as personality changes and possible increased agitation. Common neurobehavioral changes include: a tendency to blame others for one’s faults, suspiciousness, impulsiveness, constant complaining, lack of self-control, and lack of

Huntington’s is a fatal progressive disease that is associated with both musculoskeletal and neuromuscular changes which result in abnormal movements, changes in personality, and dementia. Because HD is correlated to chorea, unsteady gait and involuntary random movements, this disease is also known as Huntington’s chorea.¹ This disease has been described as having symptoms associated with Amyotrophic Lateral Sclerosis, Parkinson’s and Alzheimer’s disease all at the same time.²

Huntington’s Disease is caused by a defective gene inherited from the parents, carried on chromosome 4. It is responsible for making ‘huntingtin’. Basically, it means that certain proteins needed to make brain chemicals are unable to make them in your brain as normal. This leads to damage and the death of some brain cells, called neurons, in the basal ganglia and the cortex, located in the brain. This leads to Huntington disease, and a buildup of dopamine, a chemical that is produced to make you feel good, contributes to the problem.

Named after George Huntington, Huntington’s Disease is a hereditary neurodegenerative disease. It “causes the death of specific neurons in the brain, leading to jerky movements, physical rigidity, and dementia (First).” The mutation was first mapped to chromosome 4 in 1983, becoming the first disease gene to be mapped using DNA polymorphisms (First). In 1993, a group of investigators found the gene that causes Huntington’s Disease. It is caused by a mutation in a gene located on chromosome 4 (Mennitto). The gene contains an abnormally large number of CAG (Mennitto). The gene may lengthen when passed from father to child, but not mother to child (Mennitto).

Huntington's Disease causes the progressive breakdown (Degeneration) of nerve cells in the brain. Huntington's disease has a big impact on a person's functional abilities and usually results in movement, thinking, and psychiatric disorders. When the disease develops before age 20, the condition is called juvenile Huntington's disease. An earlier emergence of the disease often results in a somewhat different set of indications and faster disease progression. Huntington’s Disease mostly causes movement, thinking, and psychiatric disorders with a wide spectrum of signs and symptoms. Some symptoms include Movement Disorders which can lead to involuntary jerking or writhing movements and difficulty with the physical production of speech or swallowing. Thinking Disorders which make you have a lack of awareness of one's own behaviors/abilities and slowness in processing thoughts or have trouble finding words. It also can make you have Psychiatric Disorders which can make you have a feeling of sadness or irritability, Fatigue, and loss of energy, and frequent thoughts of death, dying or suicide. Now for the causes of disease, Huntington's disease is caused by an inherited defect in a single gene. Huntington's disease is an autosomal dominant disorder, which means that a person needs only one copy of the defective gene to develop the disease. With the exception of genes on the sex chromosomes, A person inherits two copies of every gene, one copy from mom and one from dad. A parent with a defective gene could pass along the defective copy of the gene or the healthy copy. Each child in the family, Therefore, Has a 50 percent chance of inheriting the gene that causes the Genetic

The most common reason people die is due to infection, such as pneumonia, or it is also possible people will die from suicide (Kantor, 2015). The risk of suicide for people with Huntington’s Disease is the greatest before they become diagnosed

Huntington disease is a degeneration of the nervous system. It usually occurs in the older part of someone life. As the disease becomes worse it could cause uncontrollable movements in the body. Because the disease causes loss of brain cells, a person can lose memory. It can also contribute to depression. It takes about to ten to twenty years after the first signs of the disease for death to follow.

Huntington's Disease Society of America state, "Huntington's disease is a genetic disorder that causes the breakdown of nerve cells in the brain. It ruins a person's physical and mental abilities during their prime working years." Huntington's is known as the a family disease because every child of a parent