Marfan Syndrome


Marfan syndrome is a rare connective tissue disorder that affects many organ systems, including the skeleton, lungs, eyes, heart, and blood vessels. Connective tissue holds body tissues together and provide support for many structures in the body. In Marfan syndrome, there is something wrong with the chemical make-up of the connective tissue. This can result in problems with the eyes, blood vessels, heart, spine, and lungs.

It is estimated that at least 1 in 5,000-10,000 people in the United States have the disorder.


Marfan syndrome is caused by a defect in the gene that controls a protein important for the development of connective tissue. In almost all cases, the defective gene is inherited. In very rare cases, the defect can be caused by a mutation during the formation of sperm or egg cells. The defective gene reduces production of a protein called fibrillin-1, whose absence allows excess action of a body growth substance called transforming growth factor-beta (TGF). Excess TGF leads to a number of the symptoms and complications of Marfan syndrome.

Risk Factors

A risk factor is something that increases your chance of getting a disease or condition.

Risk factors include:

Family members with Marfan syndrome (the child of a person with Marfan syndrome has a 50% chance of inheriting the condition) Advanced age of parents at the time of a child's birth Symptoms Symptoms of Marfan syndrome range from mild to severe and can affect one or many parts of the body. Some symptoms may be evident at an early age and others may develop later in life. Some symptoms may worsen with age. Symptoms are listed according to parts of the body they affect: Heart and Blood Vessels Abnormalities of the heart valves and blood vesselsthe two leaflets of the mitral valve may billow backwards when the heart contracts ( mitral valve prolapse ). This can lead to leakage of the mitral valve or irregular heart rhythm. Weakened or stretched aorta, the artery that leads from the heart. Eyes Dislocated eye lenses Myopia nearsightednesss), sometimes severe Glaucoma Cataracts Detached retina Bones Tall slender build Loose joints Unusually long legs, arms, fingers, and toes Crowded teeth Malformed breastbone Curved spine High, arched palate in the mouth Risk for bone thinning ( osteoporosis ) in adult life Back
Weakening of the supportive tissue of the spine with age Back pain Lungs Lung collapse (rare) Diagnosis Marfan syndrome is difficult to diagnose because there is no specific laboratory test for the condition. A doctor can diagnose Marfan syndrome by: Observing the symptoms Performing a complete physical exam Carefully studying your medical history and your family's medical history Performing tests such as: Echocardiogram a test that uses high-frequency sound waves to examine the size, shape, and motion of the heart Complete eye examination If you have Marfan syndrome: Your first-degree relatives (parents, brothers, and sisters) should be screened for the disorder. Treatment There is no cure for Marfan syndrome. Treatment is aimed at preventing or reducing complications or symptoms. Treatment may include: For the Heart and Blood Vessels Regular monitoring of the heart and aorta with check-ups or echocardiograms Avoidance of strenuous exercise or contact sports as directed by your doctor Preventive antibiotics before medical procedures or dental cleaning for patients with valvular or aortic problems Heart medications such as beta-blockers. Studies in animals with a comparable defect in fibrillin-1 show that a blood pressure medication called Losartan can prevent the occurrence of aortic aneurysm , the most serious risk in Marfan syndrome. Human studies will soon be underway to see if Losartan will be equally effective in reducing the risk of this unfortunately not uncommon complication. Surgery to repair or replace a defective heart valve or aorta For the Eyes
Regular eye examinations to check for eye problems Eyeglasses or contact lenses to correct myopia or problems with the eye lens Eye surgery for severe problems For the Bones Regular physical exams to monitor for bone problems, especially during adolescence Orthopedic brace or surgery in severe cases For the Back Exercises or medication to relieve pain caused by spinal weakness For the Lungs Avoid smoking Prevention There are no guidelines for preventing Marfan syndrome. You can contact a genetic counselor to determine the risk of your child inheriting Marfan's syndrome should you decide to have children. RESOURCES: American Academy of Family Physicians The National Marfan Foundation CANADIAN RESOURCES: Canadian Family Physician The Canadian Marfan Association References: American Heart Association website. Available at: . Mayo Foundation for Medical Education and Research website. Available at: . The Merck Manual of Medical Information . 17th ed. Simon and Schuster, Inc.; 2000.
Moura B, Tubach F, Sulpice M, Boileau C, Jondeau G, Muti C, et al; Multidisciplinary Marfan Syndrome Clinic Group. Bone mineral density in Marfan syndrome. A large case-control study. Joint Bone Spine . 2006 Sep 14 National Institute of Arthritis and Musculoskeletal and Skin Disorders website. Available at: . Travis J. Medicine. Old drug, new hope for Marfan syndrome. Science . 2006 Apr 7;312(5770):36-7. Last reviewed October 2007 by Mark A. Best, MD, MPH, MBA, FCAP, FASCP Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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