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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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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is like that. Have you ever heard of something called Marfan syndrome or MFS? It is a genetic disorder that about one in every five thousand people have and there is a fifty percent chance that it can be passed on to the next generation ("What Is Marfan Syndrome?"). Marfan syndrome is an abnormal condition characterized by elongation of the bones‚ and abnormalities in the cardiovascular system and the eyes (Hamilton). Marfan syndrome is a genetic disorder that can be inherited from ancestors and
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Victoria Haskins Biology Honors Mr. Kelly March 6th‚ 2017 Edwards Syndrome Edwards syndrome‚ also known as Trisomy 18‚ is a condition caused by a mistake in meiotic cell division resulting in an extra chromosome 18 in a developing baby (Source 1). This condition disrupts normal development‚ potentially fatally‚ even before birth (Source 1). Major characteristics of the disorder include a delay in growth‚ a low birth weight‚ and other major medical complications (Source 1‚ Source 3). Professor of
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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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Kartagener’s syndrome is an autosomal recessive disorder affecting the cilia within the body. Autosomal recessive means that one or more of both the parents’ genes responsible for encoding the cilia’s structure are mutated. This essay will focus on the etiology‚ clinical manifestations and anatomic alterations while also exploring diagnostic and treatment modalities. Cilia are the tiny hair-like structures found in many organ systems including the respiratory and reproductive systems. It was diagnosed
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Feed Join SCCM on Facebook Follow SCCM on Twitter SCCM on YouTube SCCM on FriendFeed Bookmark SCCM MySCCM SCCM Home LearnICU eCommunity MyICUCare Contact Us Go * Society of Critical Care Medicine (SCCM) SCCM > Publications > Critical Connections > Archives > December 2010 > Nursing Care Skip navigation links About SCCM Expand About SCCM Annual Congress Expand Annual Congress Conferences Expand Conferences FCCS‚ FDM & PFCCS Expand FCCS‚ FDM & PFCCS Membership Expand Membership
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Asperger’s Syndrome In today’s society‚ Asperger’s Syndrome is being talked about‚ and seen‚ more than ever‚ from television shows‚ such as Parenthood‚ to magazine articles‚ and of course in the inclusive classroom. Throughout this paper we will be looking at where Asperger’s Syndrome originated‚ some of the characteristics and causes‚ as well as ways in which teachers and parents can better deal with a child that has Asperger’s Syndrome. Asperger’s Syndrome is found under Autistic Spectrum
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1. A physician is called to the intensive care unit to provide care for a patient who received second- and third-degree burns over 50 percent of his body due to a chemical fire. The patient is in respiratory distress and is suffering from severe dehydration. The physician provides support for two hours. Later that day the physician returns and provides an additional hour of critical care support to the patient. 2. A 23-month-old infant with a heart condition presented to the ED. The physician examined
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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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