Marfan syndrome 1 THE DISCOVERY OF MARFAN SYNDROME Biology 111 Index 1517 Marfan syndrome page 2 During this past spring semester we have covered many systems of the body in Biology. Covering the endocrine system I learned of a disorder called Marfan syndrome that affected former president Abraham Lincoln. The understanding of Marfan syndrome has evolved over the past few decades. Many diseases are named after the primary researcher or the person who discovered the disease and proclaimed
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Williams syndrome also recognized as Williams-Beuren syndrome is a genetic disorder caused by a deletion of more than twenty five genes from chromosome 7. Although Williams syndrome is often non-hereditary‚ the chances of the syndrome being passed on if an individual with Williams syndrome has a child are fifty percent. Individuals born with Williams syndrome often possess distinctive facial features which make the syndrome easily recognized. These features include wide spaces between their teeth
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Marfan Syndrome Wesley Thompson Jim Hutchins Biomedical Core 1110 November 19‚ 2011 Marfan syndrome is a variable‚ autosomal-dominant disorder in the connective tissue with distinct physical characteristics. The principal features affect the cardiovascular system‚ eyes and skeleton. This condition affects the connective protein that forms the structural support for tissues outside the cell. This disease is a result of a faulty makeup of chromosomes. Since MFS (Marfan Syndrome) is an
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COMMUNITY COLLEGE DEPARTMENT OF NURSING CLINICAL ASSESSMENT TOOL Subjective Data (Basic Conditioning Factors) Student: Date of Care: 10/03/09 Patient’s Initials: P. V. Age: 37 Room #: 3114 Bed 1 Allergies: Food: NKA Gender: F Medications: NKA Environmental: NKA Admitting Diagnosis: Pancreatitis Developmental Stage (Erickson and Havinghurst): (List Developmental stage and tasks‚ assess each task) 1. Selecting a mate: Although patient
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Reye Syndrome Reye Syndrome is an extremely rare‚ non-contagious disease thought to be triggered by aspirin use. The actual origin of the disease is unknown. Reye’s Syndrome‚ occasionally called Reye-Jacobsen’s Syndrome‚ is known to follow any viral infection. Two of the most common viral infections it precedes is influenza‚ "the flu"‚ and chicken pox. A now-familiar warning on bottles of aspirin‚ most notably Tylenol‚ is not to give Tylenol to a child who is recovering from the chicken
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President Obama’s health care plan‚ Patient Protection and Affordable Care Act (PPACA)‚ commonly known as ObamaCare‚ ensures that all people have some type of health insurance and that insurance agencies are not allowed to discriminate against individuals with preexisting health conditions. Although the idea of everyone having access to health care via health insurance is ideal and worth working towards‚ the ObamaCare program is not advantageous for the majority of Americans because of higher tax
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Marfan Syndrome Have you ever wondered about the diseases that you can get from your parents? One of these major diseases that can change someone’s life is called the Marfan Syndrome. Marfan Syndrome is a disorder of connective tissue that is inherited from the parents. The bones and circulatory system are usually the parts of the body that are longer and the ones that are changed because of the disease. There are many things that can cause a disease. Marfan syndrome is caused by a mutation
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Cushing’s Syndrome Cushing’s Syndrome is a condition that results from chronic exposure to excessive amounts of glucocorticoids circulating in the blood stream for an extended period of time. The disease was first reported by Harvey Cushing over one hundred years ago‚ yet the condition still plagues endocrinologists today. Reasons for this difficulty include the vast amount of often vague symptoms that the syndrome presents‚ most of which are found in a plethora of other conditions as well‚ combined
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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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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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