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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Ophelia Syndrome Study Skills November 12‚ 2012 In the essays of Diagnosing and Treating Ophelia Syndrome and Everybody is Ignorant on Different Subjects two topics are discussed which are related‚ in that they both have to do with learning and being able to think as an individual. The Ophelia Syndrome is not processing the ability to create one’s own opinion. Ophelia is a character in the play Hamlet. She is described as a helpless child and has a “Lord” or authoritative figure that forces
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captors. Although not deeply documented a form of the syndrome may have afflicted slaves after being freed under the Emancipation Proclamation. The master presided over the land the slaves were allotted to‚ no outside contact may be made‚ escape often had penalty of death‚ and all facilities were provided by the master. Some slaves were against the idea of leaving slavery‚ thereby entranced by the syndrome. ( Krasnec) Stockholm syndrome is a term used to describe when a kidnap or barricade victim
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DOWN SYNDROME TRISOMY 21 BY: CYNTHIA AGUILAR 11/05/2012 Down syndrome affects many people in this world. Not only does it affect the person diagnosed as Downs‚ but it also affects their family and everyone around them. There are physical characteristics that help you identify somebody with Downs. There are also some health concerns that you need to worry about. Down’s Syndrome‚ it is one of the most frequently occurring chromosomal
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Metabolic syndrome Insulin resistance syndrome; Syndrome X Last reviewed: June 2‚ 2012. Metabolic syndrome is a name for a group of risk factors that occur together and increase the risk for coronary artery disease‚ stroke‚ and type 2 diabetes. Causes‚ incidence‚ and risk factors Metabolic syndrome is becoming more and more common in the United States. Researchers are not sure whether the syndrome is due to one single cause‚ but all of the risks for the syndrome are related to obesity. The
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In this imbalance research paper‚ it will discuss and explain of a certain disorder in the nervous system called Tourette’s syndrome. It will also acknowledge the current studies and research that can potentially find a way to cure this disorder. First‚ we need to more knowledgeable about this disorder. Tourette’s syndrome “is a nervous system (neurological) disorder that starts in childhood. It involves unusual repetitive movements or unwanted sounds that can’t be controlled (tics)” (Mayo Clinic
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Cushing Syndrome Sometimes called hypercortisolism. Cushing s syndrome is a hormonal disorder caused by prolonged exposure of the body s tissues to high levels of the hormone cortisol. Causes Pituitary Adenoma Pituitary adenomas cause 70 percent of Cushing s syndrome cases‚ excluding those caused by glucocorticoid use. These benign‚ or noncancerous‚ tumors of the pituitary gland secrete extra ACTH. Most people with the disorder have a single adenoma. Ectopic ACTH Syndrome Some benign
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01/29/2003. The SSA granted disability benefits because of borderline intellectual functioning and pervasive developmental disorder. She had a history of Apert’s syndrome
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Restless Legs Syndrome I. History of Disorder Restless legs syndrome is a neurological disorder that has been studied for hundreds of years. The earliest documentation of the syndrome was recorded nearly 400 years ago by Thomas Willis‚ a 17th century English physician who served King Charles II. Willis described cases of people having trouble sleeping because of constant contractions of tendons in the legs. Soreness resulted from these contractions and would hinder sleep for days at a time. The
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Marfan’s Syndrome Marfan syndrome is an inherited connective-tissue disorder transmitted as an autosomal dominant trait. It is distributed worldwide‚ has a high prevalence rate and has pleiotropic manifestations‚ meaning one gene influences multiple traits that do not seem to be related. Mutations of the FBN1 gene on the 15th chromosome (more specifically chromosome 15q21.1) cause Marfan syndrome. The FBN1 gene is coded to make a glycoprotein called fibrillin-1
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