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Is a potentially serious disease of connective tissue in the body. The result is that the normal functions of the heart and cardiovascular system, bones, ligaments and the lungs are compromised. Defects in the fibrillin gene are the reason for the resulting disorder. In most cases it is inherited through the family tree, but a smaller number of patients who have no family history of disease. Vision in people with Marfan syndrome must be monitored .
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