Marfan Syndrome history, symptoms, and cures, includes bibliography

Marfan Syndrome is a heritable disoblige of the connector tissues that affect many organs such as the eyes, lungs, skeleton, heart, and blood vessels. The condition affects some(prenominal) genders of any race and ethnicity groups. An estimation of at least 200,000 flock in U. S contract Marfan Syndrome or a link up connective tissue dis edict. 1. Margan Syndrome was first discovered in 1896 by a French pediatrician, Antoni Bernad Jean Marfan, when he was looking at a five and a half year old girl with abundant thin limbs. However, this disease is suspected to find been around for a immense time. The famous Eygptian pharoh, Akhenaten, who reigned from 1356-1332 BC, had himself portrayed with farsighted digets and a curved spine, both of which argon honey oil symptoms of the disease. tempestuous seat Lincoln was in like manner speculated to be a victim of the disorder. In 1991, the chromosome, gene and component of connective tissue in which the revolution for the Marfan syndrome is located was identified. 2. The most common symptoms of marfan syndrome are associated with the cardiovascular system, the skelton, and the eyes. Victims of the disease are often puddle irregular heart musical rhythm and outpouring in the mitral valve due to the mitral valve prolapse. They also have a wider and more fragile aorta that in the long term is prong to leakage and dissection. Marfan syndrome patients often have skeletal manifestations including the bender of the spine, abnormally determine chest, loose jointedness and disproportionate growth, often resulting in tall stature. In addition, the patients are often near spy and 50 portion have dislocation of the ocualr lens. Shorter life spans are also common. However, the Marfan Syndrome is toilsome to diagnose due to the lack of ad hoc laboratory tests for the condition. Also, the characteristics of the disorder vary greatly... If you want to get a full essay, order it on our website: BestEssayCheap.com

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