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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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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Dysexecutive Syndrome occurs when there is a loss of executive brain function. The term was first coined by Alan Baddeley and may result from physical trauma such as a blow to the head‚ a stroke or other internal trauma. Executive brain function‚ which includes insight‚ judgment‚ planning and initiative‚ makes it possible for humans to successfully manage the problems of everyday life. These functions allow individuals to carefully navigate day to day activities‚ make certain decisions‚ while
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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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the disease. Progeria Research Foundation also funds medical research that is specifically aimed at finding the cause. Treatments and cures for this syndrome are more reasons that the foundation funds research for the disease (How PRF was formed). Progeria is an outcome of a fault in the Lamin A(LMNA) gene (Hutchinson-Gilford Progeria Syndrome 2012). The LMNA gene has codes that are for two proteins‚ Lamin A and Lamin C. These proteins play a big role in stabilizing the inner membrane of
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What affected my life the most were the traumatic experiences of my childhood that have shaped my entire life. I don’t often speak about what goes on in my life or my past because I feel that it is better to keep things to myself then to show people that I am weak. I grew up in an abusive home my family changed because of certain events that took place within our family. I always remember being more depressed than other children. I just wanted to be normal and pretty my entire life. As time went
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Hunter Syndrome Hunter syndrome is a rare genetic disease that almost always occurs in males. This incurable disease is also called mucopolysaccharidosis II (MPS II). This disorder is caused by the deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). This enzyme is needed to successfully break down glycosaminoglycans‚ as part of the body’s normal recycling and renewal process. In a person with Hunter syndrome‚ enzyme I2S is missing or not working correctly. It is the accumulation
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Tourette Syndrome is a neurological disorder that is characterized by sudden repetitive and involuntary movements or vocalizations that are generally termed “tics”. These tics can have different degrees of intensity ranging from simple to complex. Simple motor tics are brief‚ sudden‚ and repetitive movements that involve a limited number of muscle groups. They include facial grimacing‚ eye blinking and other eye movements‚ and head or shoulder jerking. Simple vocalizations include repetitive sniffing
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