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Jeremy Phillips Term Paper

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Twenty minutes before my shift ended, Jeremy Philips walked into my office. He is 44 years old and weighs 175 lbs. He starts to explain what his symptoms consist of and I sit down knowing what disease he has. I brace myself for a long and heartbreaking case. Jeremy Philips explained that he was been having a facial tic for several weeks. He also has been slurring his words and his speech has been slowing down. Also, he has been having mood swings. As I write down his symptoms, I ask him if he has any history of mood swings or depression in his family. He tells me that his father committed suicide at 49 years old and he was treated for depression and is no longer on medication. I write this information down and start to think of what tests to run. I ask him to follow me for an MRI. After, I look at his results and there are structural changes at sites of the brain that are affected by Huntington’s disease. I take him back to my office for a sample of his blood. I take the sample and run it for genetic testing which analyzes DNA for the Huntington’s disease mutation by counting the number of CAG repeats in the huntingtin gene. Normal people have less than 28 repeats of the gene. Jeremy has over 40 repeats. This diagnosis him with Huntingtons disease. …show more content…
It deteriorates an intividual’s mental and physical abilites. Symptoms for this disease appear between the ages of 30 and 50 years old. the disease worsens from a period of ten to twenty-five years. Over time the disease affects the persons ability to reason, walk and speak. HD is a family related disease. Each child born from a parent with HD has a 50 percent chance of carrying the gene. I tell him that aproximately 30,000 Americans have the disease and more that 200,000 are at risk of inheriting it. Roughly five to seven people are affected per 100,00

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