"Liver disease" Essays and Research Papers

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    Gaucher's Disease

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    Gaucher ’s Disease is an autosomal metabolic disorder. This means that it is inherited from both parents. For a child to develop the disease both the mother and the father must to carry the necessary gene. If in fact the child inherits the disease he or she will experience problems with the liver‚ spleen‚ lungs‚ bone marrow‚ and in some cases the brain. The disease is caused by excessive amounts of a fatty substance called glucocerebroside. Glucocerebroside accumulates in the organs when there is

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    Bio Disease

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    to the brain. It can lead to the hepatic encephalopathy that is known as a fatal brain disorder. * Liver: Basically‚ in taking of alcohol means in taking of toxins. Liver tries to get rid of these toxins by breaking them but the liver turns out fatty. Alcohol results in an increase in the fibrous tissue that prevents the blood to reach the cells in the liver. All this result the liver to die because it doesn’t get appropriate amount of blood to survive. * Kidneys: Alcohol can damage

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    C Travis F. Shoffner American Military University Abstract This research paper looks at the infectious disease hepatitis C. The research draws upon primary sources including medical websites and electronic newspaper articles. The goal is to inform and describe the disease‚ cite current infections and death statistics related to it. The paper will also explain how the disease affects the body and discuss current and future treatment options. This research will provide valuable information

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    Rhesus disease is an infant wellbeing condition that is brought on by an incompatibility between the mother’s blood classification and the baby. Here’s the significance: Most individuals have Rh-positive blood‚ implying that they create an Rh protein on the surface of their red platelets. Also called erythroblastosis fatalism during pregnancy. In the newborn‚ the resulting condition is called hemolytic disease of the newborn (HDN). Be that as it may‚ around 15 percent of Caucasian ladies and around

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    Wilsons Disease

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    Wilson’s Disease is a genetic disorder that is fatal unless detected and treated before serious illness develops from copper poisoning. Wilson’s Disease affects one in thirty thousand people world wide. The genetic defect causes excessive copper accumulation. Small amounts of copper are essential as vitamins. Copper is present in most foods‚ and most people get much more than they need. Healthy people excrete copper they don’t need‚ but Wilson’s Disease patients cannot

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    also serves as a large source of free radical generation in Alzheimer’s disease. Another possible mechanism involved in Alzheimer’s disease is the creation and accumulation of glutamate hydroxyl radical (Behl et al.‚ 1992) and also the over production of superoxide dismutase. This leads to the accumulation of hydroxyl radical produced from the conversion of hydrogen peroxide (H2O2). A characterization of Alzheimer’s disease is by the loss of the amyloid B (beta) protein which is in the neocortex

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    The Wilson's Disease

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    The Wilson’s Disease The Wilson’s disease is a genetic disorder of the thirteenth chromosome. This disease is an inherited disease and it is mostly likely to be in all of the offspring if a parent had it. It is the unnecessary increase of copper in the liver and brain. This is cause by a defect in the transport of copper. Wilson’s disease is a rare autosomal recessive disorder of the copper transport resulting in the copper buildup. It is also known as Hepatolenticular Degeneration as the

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    Liver Cancer Essay

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    Liver cancer is a disease which begins in the cells of your liver. There are different forms of liver cancer. There is primary liver cancer‚ which arises in the liver or by cancer which forms in other parts of the body and then spreads to the liver. Most liver cancer is secondary or metastatic‚ which means it started elsewhere in the body. The most common form of liver cancer is hepatocellular carcinoma‚ which begins in the main type of liver cell (hepatocyte). The other type is cholangiocellular

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    Wilsons disease

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    April 22‚2014 Disease fact sheet What is Wilson disease? Wilson disease is a genetic disorder that prevents the body from getting rid of extra copper. A small amount of copper obtained from food is needed to stay healthy‚ but too much copper is poisonous. In Wilson disease‚ copper builds up in the liver‚ brain‚ eyes‚ and other organs. Over time‚ high copper levels can cause life-threatening organ damage. Pathophysiology and clinical features of Wilson disease Wilson disease is an autosomal

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    An investigation to compare the reaction rates between potato and hydrogen peroxide against liver and hydrogen peroxide through loss in mass. Background information: Catalase is an enzyme that is found in all cells. This means that it is an intracellular enzyme. And enzyme is a biological catalyst. A catalyst is some thing that speeds up a reaction without being changed itself. Because of this enzymes and catalysts can be used again and again. Enzymes are protein chains that have a primary‚ secondary

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