Info Eye Problems Linked to Marfan Syndrome and Fixes
Marfan syndrome is a genetic disorder affecting the body's connective tissue, leading to abnormalities in the heart, eyes, blood vessels, and skeleton.
It's caused by mutations in the FBN1 gene, which codes for fibrillin-1 protein.
Common symptoms include tall stature, long limbs, joint hypermobility, and vision problems.
Cardiovascular complications, such as aortic aneurysms, are a leading cause of morbidity and mortality.
Diagnosis is often made through genetic testing and physical examination.
Treatment involves regular monitoring, medication, and surgery to prevent or repair cardiovascular complications.
Beta-blockers and other medications can help manage symptoms and slow disease progression.
Lifestyle modifications, such as avoiding contact sports, can help reduce the risk of injury and complications.
Early diagnosis and treatment can significantly improve outcomes and life expectancy.
Genetic counseling is recommended for families with a history of Marfan syndrome.