It affects the body's production of fibrillin, which is a protein that is an important part of connective tissue.
marfan syndrome is genetic disorder of connective tissue of the body. it cause a mutation of the gene that produces the protein fibrillin.
Marfan syndrome
Marfan syndrome is found in 1 in every 5,000 - 10,000 births. If one of your parents has Marfan syndrome, you have a 50% chance of having Marfan syndrome.
Yes. Marfan syndrome is caused by a defect (or mutation) in the gene that tells the body how to make fibrillin-1.
Marfan's Syndrome is inherited in an autosomal dominant pattern. This disease is a disorder that affects the connective tissue in many parts of the body.
Yes, Marfan syndrome is autosomal dominant.
Marfan Syndrome is a medical problem with the Conective Tissue.
Some of the effects on a person with Marfan's syndrome might be that they would have bad eyesight, they would be abnormally tall (7ft), they might also have a long face and loose joints.
Unfortunately no. The mutation that causes Marfan syndrome is found in every single cell in the body. It would be impossible to replace it in every cell.
Marfan syndrome affects three major organ systems of the body: the heart and circulatory system, the bones and muscles, and the eyes.
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.