"Blue baby syndrome" Essays and Research Papers

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    Designer Babies

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    Critical Review of Designer Babies: The Pros and Cons of Genetic Engineering Author: Siew Yang Yi Yin Ren. Designer Babies: The Pros and Cons of Genetic Engineering. MURJ Volume 12‚ Spring 2005. Genetic engineering is the modification of an organism’s genome through direct human manipulation of the DNA using modern technology. Although classical genetic methods using selective breeding has been done by humans since thousands of years ago‚ the manipulation of genome of organism through advance

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    Turner Syndrome

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    published the first report on the symptoms of Turner Syndrome. It was published as “A Syndrome of Short Stature‚ webbed beck and infantilism”. It was a report on seven girls who shared similar features to each other. Dr. Turner helped with the advancement of treatment for the girls with the syndrome. He did this by pioneering the use of exogenous sex steroids for treating ovarian failure (“Years of Medical Advances in Turner Syndrome”) . Today‚ Turner Syndrome occurs in 1 in 2‚500 females worldwide. 15% of

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    Down's Syndrome

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    Down’s Syndrome Abstract This research is aimed at getting theoretical and practical knowledge about Down’s Syndrome. Psychological aids such as observation‚ Informal Interviews and case histories were used to gather information for this project. The conclusion drawn was that it is possible for individuals suffering from Down’s Syndrome to lead a fairly normal and highly satisfying life if they are provided with a loving and nurturing environment at home. Introduction The aim of this paper

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    Noonan Syndrome

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    Noonan Syndrome Nicole Mitchell Dr. Hendricks Principles of Biology 1114 April 19‚ 2013 Mostly everyone in the world has heard of some type of genetic disorder. But most people haven’t even heard or understand about Noonan Syndrome. Noonan syndrome is a genetic disorder characterized by distinctive facial features‚ developmental delay‚ learning difficulties‚ short stature‚ congenital heart disease‚ renal anomalies‚ and bleeding difficulties. Noonan syndrome affects a good percent of the world

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    Klinefelter Syndrome

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    Klinefelter Syndrome is a syndrome in which a person has an additional X-chromosome. It is not life consuming‚ but rather people who have this syndrome can live perfectly normal lives proper treatment and care‚ if precautions are taken early on. Dr. Harry Klinefelter in 1942 first identified the syndrome. Now some may ask what Klinefelter syndrome is. Klinefelter syndrome is a syndrome in which a person inherits an extra X-chromosome making their genetic makeup xxy instead of the normal How it occurs

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    Metabolic syndrome

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    Running head: METABOLIC SYNDROME Metabolic Syndrome James Doucette College of Western Idaho Abstract Metabolic syndrome is an emerging diagnosis in the medical field that has effects on patient care. Becoming familiar with it and having it become a common part of patient care will‚ if used appropriately will increase the lives of those who have become affected with or are at risk of becoming diagnosed with metabolic syndrome. Metabolic syndrome is a constellation of risks

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    Sundowning Syndrome

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    Sundowning Syndrome Etiology and Treatment 12/3/2010 Anatomy & Physiology sundowning syndrome: etiology and treatment An escalation in disruptive behaviors in the late afternoon and early evening among institutionalized patients suffering from dementia and Alzheimer’s disease has been a recognized phenomenon for over 60 years (Bachman & Rabins‚ 2006). The timing of the onset of disruptive behaviors has led to calling this phenomenon sundowning‚ sundowning syndrome‚ and nocturnal delirium

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    Munchausen Syndrome

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    Munchausen Syndrome 1 Running head: Munchausen Syndrome Munchausen Syndrome by Proxy 5 References Author: Ibrahim Abdulhamid‚ MD‚ Assistant Professor of Pediatrics‚ Wayne State University; Director of Pediatric Pulmonary Medicine‚ Clinical Director of Pediatric Sleep Laboratory‚ Children ’s Hospital of Michigan Coauthor(s): Patricia T Siegel‚ PhD‚ Assistant Professor‚ Departments of Pediatrics‚ Psychiatry and Behavioral Neurosciences‚ Wayne State University School of Medicine Contributor

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    Alagille Syndrome

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    Alagille Syndrome Abstract Alagille syndrome is a genetic disorder passed either by the parents or due to a genetic mutation(s). The liver is the affected region of the body. The liver has a lower count of bile ducts within the liver resulting in liver damage due to buildup of bile. If the liver stops working a transplant is needed for the patient to survive. This disorder also affects many other systems of the body. Treatment options include either use drugs or a liver transplant. There is

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    Nephrotic Syndrome

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    Nephrotic syndrome is a group of symptoms including protein in the urine‚ low blood protein levels‚ high cholesterol levels‚ and swelling. The urine may also contain fat‚ which can be seen under the microscope. Nephrotic syndrome is caused by various disorders that damage the kidneys‚ especially the basement membrane of the glomerulus. This causes abnormal excretion of protein in the urine. This condition can also occur as a result of infection‚ use of certain drugs‚ cancer‚ genetic disorders

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