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What is Understanding Marfan Syndrome Symptoms about?

Marfan syndrome is a genetic disorder that affects connective tissue and can impact the heart, blood vessels, bones, eyes and lungs. It is caused by a mutation in the FBN1 gene that results in abnormalities in connective tissue. Symptoms can range from mild to severe and include long limbs, flexible joints, curved spine and eyeglass prescriptions. It is a dominant genetic trait, so if one parent has it there is a 50% chance their child will have it as well. While there is no cure, treatment focuses on monit

Author

Mark Thomas Johnson

Language

EN