What Is Marfan’s Syndrome? Marfan’s syndrome is an inherited connective tissue disorder that affects normal body growth. Connective tissue provides support for your skeletal structure and all organs of your body. Any disorder that affects your connective tissue (such as Marfan’s syndrome) will impact your entire body, including your organs, skeletal system, skin, eyes, and heart. Obvious physical characteristics of this disorder include being tall and lanky, and having loose joints, large and flat feet, and disproportionately long fingers. This disorder occurs among people of all ages and races. It’s found in both men and women. According to the Marfan Foundation, the syndrome occurs in about one in 5,000 people. Recognizing the Signs of Marfan’s Syndrome Symptoms of this disorder may show up in infancy and early childhood, or later in life. Some symptoms may worsen with age. Skeletal System This disorder shows itself differently in different people. The visible symptoms occur in your bones and joints. Visible symptoms may include: unusually tall heightlong limbslarge, flat feetloose jointslong, thin fingersa curved spinea chest bone (sternum) that sticks out or caves inwardcrowded teeth (caused by an arch in the roof of the mouth) Heart and Blood The more invisible symptoms occur in your heart and blood. Your aorta, the large blood vessel that transports blood from your heart, may become enlarged. An enlarged aorta may cause no symptoms. However, it carries the risk of a life-threatening rupture. Seek medical assistance immediately if you’re having chest pains, breathing problems, or an uncontrollable cough. Eyes People with Marfan’s syndrome often have eye problems. About one in six people with this condition have “partial lens dislocation” in one or both of their eyes. Becoming severely nearsighted is also common. Many people with this condition need eyeglasses or lenses to correct vision problems. Finally, early-onset cataracts and glaucoma are also much more common in people with Marfan’s syndrome, compared to the general population. What Causes Marfan’s Syndrome? Marfan’s syndrome is a genetic or inherited disorder. The genetic defect occurs in a protein called fibrillin-1, which plays a large role in the formation of your connective tissue. The defect also causes overgrowth in bones, resulting in long limbs and significant height. There’s a 50 percent chance that if one parent has this disorder, their child will also have it (autosomal dominant transmission). However, a spontaneous genetic defect in their sperm or egg can also cause a parent without Marfan’s syndrome to have a child with this disorder. This spontaneous genetic defect is the cause of about 25 percent of cases of Marfan’s syndrome. In the other 75 percent of cases, people have inherited the disorder. Diagnosing Marfan’s Syndrome Your doctor will typically begin the diagnostic process by reviewing your family history and conducting a physical exam. They can’t detect the disease through genetic testing alone. A complete evaluation is necessary. It typically includes an examination of your skeletal system, heart, and eyes. Typical exams include: an echocardiogram, which is used to examine your aorta for enlargement, tears, or aneurysms (bubble-like swelling due to weakness in the walls of the artery)an electrocardiogram (EKG), which is used to check your heart rate and rhythma magnetic resonance imaging (MRI) test, which is performed in some people to look for lower back problemsan eye exam, which allows your doctor to examine the overall health of your eyes, to test how acute your sight is, and to screen for cataracts and glaucoma. Treatments for Marfan’s Syndrome Marfan’s syndrome can’t be cured. Treatments typically focus on lessening the impact of various symptoms. Cardiovascular Your aorta becomes larger in this condition, increasing your risk for many heart problems. It’s essential that you regularly consult with a heart specialist. If problems exist with your heart valve, medications such as beta-blockers (which reduce blood pressure) or replacement surgery may be necessary. Bones and Joints Annual checkups help to detect spine or breastbone changes. They are especially important for fast-growing adolescents. Your doctor may prescribe an orthopedic brace or recommend surgery, especially if rapid growth of your skeletal system is causing problems for your heart or lungs. Vision Regular eye exams help to detect and correct vision problems. Your eye doctor may recommend eyeglasses, contact lenses, or surgery, depending on your condition. Lungs You are more at risk of developing lung problems if you have this disorder. This is why it’s important not to smoke. If you have breathing problems, sudden chest pain, or a persistent dry cough, call your doctor immediately. Living with Marfan’s Syndrome Given the many different possible complications related to the heart, spine, and lungs, people with Marfan’s syndrome run the risk of a shorter lifespan. However, regular visits to your doctor and effective treatments can help you survive into your 70s and beyond. Physical Activity Check with your doctor before engaging in strenuous sports and physical activities. Skeletal system, vision, and heart issues may make it dangerous to participate in sports like football and other contact sports. Lifting heavy objects can also cause problems and should be avoided. How to Reduce Your Unborn Child’s Risk of Marfan’s You can undergo genetic counseling before having children if you have Marfan’s syndrome. However, about one-quarter of Marfan’s cases result from spontaneous gene defects, making it impossible to predict and prevent the disease entirely. To prevent potential pregnancy complications that result from the disease, seek medical attention and have regular checkups.
Written by: Chitra Badii
Published on: Jul 19, 2012
on: Jan 27, 2016: [Ljava.lang.Object;@3df4d4e5
This feature is for informational purposes only and should not be used to replace the care and information received from your health care provider. Please consult a health care professional with any health concerns you may have.