Marfan Syndrome

There are many different types of syndromes a person can have. A syndrome is the association of several clinically recognizable features signs / symptoms that occur.

If you were not born with Marfan syndrome, there are no ways you can get it. The syndrome is caused by mutation or defection in a gene. The gene that is defect is the connective tissue which causes too much growth of bones in the body. Connective tissues are fibers that structure the human body. This makes a person with the syndrome have a body that is shaped abnormally; most of the time long legs and arms. Although, scientist aren’t sure why overgrowth happens. However Marfan syndrome affects not just outer body parts but, ...

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When these people stretch out their arms, the with-span of their arms is much greater than their height. Other symptoms could be a narrow face, flat feet, small lower jaw, learning disability, movement of the lens of the eye from its normal position and a chest sinks in or sticks out.

Unfortunately there is no cure to Marfan syndrome yet, scientists are still working on the cure to this day. Although there are treatments people can take that will reduce complications of the syndrome. If a person decides to take medication, they should start right away; early diagnose will lead to a better outcome and prevents of the syndrome. A person with Marfan syndrome should also see their doctor(s) on a regular basis. Doctors that are recommended are an orthopedist and a geneticist. An orthopedist specializes is bones and a geneticist has special knowledge about inherited diseases. Scientists are trying to learn more by studying the genes of a person or large families affected by the ...

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Marfan Syndrome. (2011, March 28). Retrieved November 29, 2020, from
"Marfan Syndrome.", 28 Mar. 2011. Web. 29 Nov. 2020. <>
"Marfan Syndrome." March 28, 2011. Accessed November 29, 2020.
"Marfan Syndrome." March 28, 2011. Accessed November 29, 2020.
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Added: 3/28/2011 04:34:25 PM
Submitted By: skaterthing777
Category: Diseases & Disorders
Type: Premium Paper
Words: 472
Pages: 2

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