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Marfan Syndrome

Marfan syndrome is a genetic disorder that impacts the body’s connective tissue. Connective tissue holds all the frame’s cells, organs and tissue collectively. It also plays an essential role in helping the frame develop and broaden nicely. Connective tissue is made up of proteins. The protein that plays a role in marfan syndrome is referred to as . Marfan syndrome is caused by a illness  mutation within the gene that tells the body how to make . This mutation consequences in an increase in a protein known as remodeling growth issue beta, . The growth in  causes problems in connective tissues at some stage in the frame, which in turn creates the features and medical troubles related to marfan syndrome and some related situations. Because connective tissue is located during the frame, Marfan syndrome can have an effect on many specific parts of the body, as properly. Functions of the disorder are most customarily determined within the coronary heart, blood vessels, bones, joints, and eyes. Some marfan capabilities – for example, aortic enlargement the lungs, pores and skin and worried machine will also be affected. Marfan syndrome does no longer have an impact on intelligence. Human beings with Marfan syndrome are born with it, however features of the circumstance aren't usually present right away.

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Citations : 135

Journal of Genetic Disorders and Genetic Medicine received 135 citations as per Google Scholar report

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