What is Marfans Syndrome?

Marfan syndrome is a genetic mutation that takes place on the 15th chromosome. The genetic mutation can be inherited through dominant traits or occur during early development. The condition is caused by a defect in the bodies’ production of fibrillin, a special protein that is found in connective tissue throughout the body. This causes weakened connective tissue which leads to problems in places such as the eyes, the heart, and joints. Although this disorder is rare (only 1 in every 5,000 people will be diagnosed) people with Marfan syndrome can now get medical treatment to have the same lifespan as everyone else.




This is Abe Lincoln. It is suspected he had Marfan Syndrome.