Marfan syndrome is a hereditary condition that involves abnormal development of connective tissues. This disorder can affect various organ systems, including the cardiovascular system, the skeleton, and the eyes. The disease is named after French pediatrician Antoine Marfan, who first described the symptoms in a young girl, which included long limbs and joint laxity. Diagnosing Marfan syndrome is not always straightforward, as the symptoms can vary widely and are not always clear-cut. Symptoms of the disease may present at birth, but diagnosis can often be delayed until cardiac or ophthalmic abnormalities become apparent. Early detection and appropriate medical treatment are essential to prevent complications. The quality of life for individuals…