Marfan Syndrome
Marfan Syndrome is an inherited disorder of the connective tissue, which is responsible for providing strength, elasticity and support to body parts. People with Marfan Syndrome have defects in the gene that controls the production of fibrillin-1, a protein involved in the formation of connective tissue. This results in weakened and stretched connective tissue, leading to skeletal deformities like long limbs, abnormally shaped chest and loose joints. It can also affect the eyes, heart and blood vessels, leading to eye dislocation, heart valve issues and aortic aneurysms. Marfan Syndrome is life-threatening, and early diagnosis and appropriate treatment is essential to improve quality of life and reduce the risk of serious complications. Treatment includes drugs to regulate heart rate, prevent aortic enlargement, and manage chest wall deformities. Surgery may be necessary to repair heart valves or the aorta. Living a healthy lifestyle and regular monitoring are also recommended to manage Marfan Syndrome.
← Journal of Tissue Repair and Regeneration