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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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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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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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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Down Syndrome (DS) is the most common chromosomal condition in the United States‚ affecting about 1 in every 700 babies (CDC). This condition is also known as Trisomy 21‚ due to there being an extra copy of chromosome 21 (CDC). This extra chromosome results in changes in the development of the brain and body‚ which in turn can lead to cognitive and physical challenges (CDC). Some hallmark physical characteristics include almond shaped eyes that slant up‚ smaller hands and feet‚ shorter stature‚
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Cited: Board‚ A.D.A.M. Editorial. Compartment Syndrome. U.S. National Library of Medicine‚ 18 Nov. 0000. Web. 09 Oct. 2012. . [->0] - http://en.wikipedia.org/wiki/Compartment_(anatomy)
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Introduction To the Disorder Asperger’s syndrome (AS)‚ originally described by Hans Asperger in 1944 (Attwood‚ 2007‚ p. 23)‚ was historically considered a distinct high-functioning subtype of autism. It is now considered simply an autism spectrum disorder (ASD) following a change to the Diagnostic and Statistical Manual of Mental Disorders (DSM) in 2013 (Kite‚ Gullifer‚ & Tyson‚ 2013). “Autism spectrum disorders are severe disorders of development that can affect social interaction‚ communication
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Thoracic Outlet Syndrome is a complex disorder characterized by a constellation of signs and symptoms resulting from a compression of blood vessels and nerves in the thoracic outlet region where they exit the chest. The thoracic outlet is a space located between the thorax (rib cage) and the clavicle (collarbone) which contains major blood vessels and nerves. The thoracic outlet is the area through which nerves and blood vessels travel to and from the arm. Thoracic Outlet syndrome is considered
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Prader Willi Syndrome Prader Willi syndrome‚ or more commonly known as PWS is a disorder that causes “obesity‚ intellectual disability‚ and shortness in height” (Mayo Clinic). PWS is a not a common disorder. According to MNT‚ it is estimated that “one in 25‚000 people have PWS in the US and it affects an estimated 350‚000 to 400‚000 people worldwide.” However‚ PWS is the most common genetic cause of life-threatening childhood obesity that has been identified to date in genetic clinics. There is
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