Noonan Syndrome Noonan syndrome is a genetic disorder that was once known as Turner-like syndrome. It is a mutation of several genes where they develop proteins that are continuously active; which ends up disrupting the control of the cells growth and division resulting in abnormal developments of the body. Noonan syndrome can affect a person’s physical appearance in multiple ways‚ along with their mental state of mind. This syndrome equally affects males and females. Noonan syndrome was first
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Angelman Syndrome In America‚ about 6 million students are known to have some kind of intellectual disability. Intellectual disabilities are not always determined by the IQ level of an individual but rather how they react to their peers‚ self-perception‚ problem solving‚ personal care‚ etc.. It could develop before birth‚ after birth or even in one’s later life. Usually‚ these disabilities are caused by mutation in one of the chromosomes of a fetus. For example‚ some syndromes are the result of
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Exceptionality Report: Angelman Syndrome The Exceptional Child Andrea Gamber-Smith Dr. Harry Angelman discovered the disease that came to share his name‚ Angelman Syndrome in 1965. Angelman syndrome is impossible to diagnose until approximately the age of three to seven when symptoms become evident. The features of Angelman’s syndrome include a stiff body‚ little or no speech‚ constant giggling or laughter‚ and an easily excitable personality. There are
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Prevention for Noonan Syndrome looks slightly different than other disorders‚ due to the fact that it is genetically linked. With cases of NS being linked to different genetics and some cases having an unknown origin‚ it is hard to prevent the disorder from occurring. A big factor towards prevention lies in the education of the people closest to the patient‚ the community‚ and the general public. A very effective preventive way would be to administer genetic testing to the population in order to
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Münchausen Syndrome and Münchausen Syndrome By Proxy Münchausen Syndrome There are many syndromes in people’s lives. All of the sydromes have been effecting people’s health negatively in people lives since the existence of human being. One of the most interesting syndrome is Munchausen Syndrome. It is related to unreal illness. In other words‚ Some people who has münchausen syndrome can cause an illness own their own. Therefore‚ they are actually clever and have medical information. Due to their
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The primary intervention in the management of dysmetabolic syndrome consists of lifestyle modifications such as cessation of smoking‚ healthy eating of calories restricted diet and increase in physical activity (Falentin‚ 2010). In dysmetabolic syndrome‚ the main emphasis is on reducing the individual risk factors especially in patients identified as high risk of cardiovascular disease and T2DM. Riediger and Clara (2011)‚ state the importance of doctors using a screening tool for other risk factors
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Bloom’s Syndrome is a rare genetic disease known for affecting someone’s physical and genetic traits‚ this disorder can cause problems for whoever is diagnosed with it. Bloom’s Syndrome is a disease characterized by how its identified‚ its frequency‚ how it was discovered‚ its symptoms‚ and its treatments. Bloom’s Syndrome is identified as an autosomal disorder. An autosomal disorder is when the defected gene is carried on a chromosome other than one of the sex chromosomes. Bloom’s Syndrome happens
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150‚000 adults were reported with RDS meaning about one person out of 6‚800 has RDS. It is very important to be careful with this syndrome because if an infant or breathing machine tried to apply some pressure to the lungs there is a high chance of it to rupture causing air to leak making the lung collapse sinking in even farther which turns it into a more severe case‚ usually this can be seen with the help of a chest x ray
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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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Turner Syndrome Allie Fitzgerald BIOL 150 11/22/11 Turner syndrome (TS) is a genetic condition in which a female does not have the usual pair of two X chromosomes (“What is TS?”). This condition was named after Dr. Henry Turner‚ who was one of the first researchers to describe the features of Turner’s Syndrome in 1930s. TS occurs in about 1 female out of every 2‚000 female births‚ but is much more common in miscarriages. A diagnosis of TS is made through a karyotype test. This is performed
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