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Huntington's disease
Huntingtons disease summary
Huntington's disease
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I looked up Huntington’s Disease to find out more about the disorder. There is no real treatment for the disorder, so I do not see any benefit of knowing that you are going to develop the disease. I feel the distress of knowing that a gene is present and the disease is going to come in time would be worse than the symptoms starting to manifest themselves. The early symptoms can develop any time, but in most cases, they develop in between the age range of 30 – 50 years of age. The initial signs and symptoms are very subtle causing problems with coordination, involuntary movement, and memory. The person affected may develop depression or irritable moods. In the early stages, there are some medications that can help with those symptoms.
The video, “Cracking the Genetic Code,” brought for forth some great interest in knowing that the medical field and technology has advanced so much that we can know our own genetic code and if we will or develop a certain disease. But aside from the interest, the video also brought forth some heartbreaking moments for the patients in the video that have had their lives turned around due to medical illness. For example, Megan Sullivan, who was a fully functional young woman and started showing symptoms of Huntington’s disease during her college years, which reduced her functioning to where she can barely even speak for the interview. It’s hard seeing somebody that young go through those huge obstacles, or in the case of Catherine Ellton, who, in a way, was forced to speed up her life in a
Huntington's Disease and Its Ethics In “Genetics and Reproductive Risk: Can having children be immoral,” L.M Purdy discusses the notion that the recent advances in reproductive technology impose a moral obligation on individuals to prevent the birth of “affected” babies that will not have a “minimally satisfying life.” There are, however, several assumptions that the author makes in reaching the conclusion that having “affected” children is immoral. The author makes the claim that people with Huntington’s disease are unlikely to live a minimally satisfying life. It is known however, that Huntington’s disease does not take any affect until 40-50 years of age.
Many people, like myself, after watching an episode of “The Michael Jay Fox Show,” started to be come curious as to what exactly this disease is. You ask yourself; What is this disease? What causes it? Can it be passed down from generation to generation? Is there a treatment? What would your life be like suffering from this? Through my research on Parkinson’s disease, I am determined to answer these questions. I hope to have a better understanding on this disease, and how it affects the lives of patients that I might see in a hospital.
Huntington’s disease (HD) is a progressive autosomal dominant neurodegenerative genetic disorder. HD was originally named Huntington’s chorea after Dr.George Huntington, an American physician who first gave a detailed note on the symptoms and course of the disease in 1872.Recently the name has been changed to Huntington’s disease to emphasize the fact that chorea is not the only important manifestation of the disease but several non-motor symptoms are also associated with this disease.[1]
About 30,000 people in the United States have Huntington's Disease, affecting men and women equally among all ethnic and racial backgrounds (helpguide.org). While its more common in adults, juvenile Huntington's occurs in one-sixth of all cases (helpguide.org). Huntington's Disease (HD) is a devastating, hereditary disease that slowly decreases the affected person's capability to walk, talk and reason. Sooner or later, the person with HD becomes completely dependent upon others for his or her care. Huntington's Disease affects the lives of entire families immensely: emotionally, socially and economically. In this research paper, the pathophysiology, manifestation, and medical management of this disease will be examined.
symptoms are not noticeable until the person with the disease reaches their middle years, approximately 30-50. The disease progresses rapidly once the first signs start showing. Within years the symptoms will get severely worse and the person’s quality of life will drastically decrease. Some of these symptoms include uncontrollable body movements, loss of mental stability, and loss of the ability to think. In the later years of the person’s life they will need assistance wit...
Dementia can occur in relation to many different illnesses. Some of the most common of which are Huntington’s Disease,
Since the gene for HD is dominant, there is a 50% chance of a sufferer's
Huntington’s disease is named after George Huntington. This disease genetically is an inherited disorder that damages the mind and nervous system. This may affect actions of the body for example like movement, the ability to reason, awareness, and thinking and judgment. It can also affect their behavior. The word genetic is that the disorder is delivered on by each generation of offspring by special codes called genes(Patient.Co.Uk, 2011). Genes are relocated from a parent to offspring and is held to decide some characteristics of the children (Patient.Co.Uk, 2011).
Huntington’s disease Huntington's disease is a genetic disease. The signs and symptoms generally develop in midlife. People with Huntington's disease at a younger age usually are the more serious cases, and their symptoms may progress more rapidly. Huntington is harder to find in children. There are medications available to help find out the signs and symptoms of Huntington's disease, but treatments cannot prevent the decline in people’s physical and mental health.
Further symptoms can develop as the disease gets worse. These include confusion and getting lost in familiar places. For example, the patient could get lost in their local area or even their own house if the disease gets worse. Also the patient finds it difficult to make decisions and have problems with their speech. This restricts them from having conversations with other people. Another symptom is having problems moving around on their own. This means they will need assistance most of the time and looked after at all times. A major change is their personality. It can change from being happy to aggressive and being very demanding. The disease usually develops as the person ages so it will be worse at the age of 70 than at the age of 40 however, depending on the person it can
A devastating, yet rare, disease that strikes fear in families and even more so in the person that is diagnosed with this debilitating disease. Huntington’s disease can affects both mental and physical parts of the body, with only medication to slow the course of this disease, a certain level of coping and adjustment is necessary.
Huntington’s disease is an inherited condition in which nerve cells in the brain break down over time. No cure exists for the disease, but drugs, physical therapy, and talk therapy can help manage some symptoms. Testing is done by blood sample. The genetic test analyzes DNA for the HD mutation by counting the number of repeats the Huntington gene made. Part of the gene repeats itself over and over again like a stutter. The results are near 100% accurate. The disease appears around age 40.
Huntington’s disease is caused by an abnormal dominant gene. Also called Huntington’s chorea, it is a complex disorder that affects a person capability to feel, think and move. The symptoms of Huntington’s disease consist of mood swings, irritability, depression, and anger. These symptoms are likely to worsen and the disease a lot of times runs in the family. If people have at least one parent with Huntington’s disease, the chances of them inheriting it are 50-50 chance. There is also a 50-50 chance that, that same person could pass the faulty gene on to their future child. This pattern of inheritance is called "autosomal dominant". The disease could also affect a person’s judgment and other mental functions. In some cases the person could