Marfan’s syndrome is not a terminal disease. Marfan’s syndrome is a familial disorder in which the patient has a family history of inheritance, but also has a significant abnormality in appearance, a disproportionate height to weight, severe growth of the limbs and fingers and toes, and a much higher than normal height. Marfan’s syndrome is not a terminal disease and can be corrected surgically if medication is not effective. The patient’s severely disproportionate body shape affects the function of all organs, which can lead to loss of organ function and sudden cardiac death over time. Patients can participate in normal activities, and because of their height, they can participate in sports and become athletes, but when there is organ dysfunction, active surgery is required.