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.
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 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.
Dislocated eye lenses
Myopia nearsightednesss), sometimes severe
Tall slender build
Unusually long legs, arms, fingers, and toes
High, arched palate in the mouth
Risk for bone thinning ( osteoporosis ) in adult life
Weakening of the supportive tissue of the spine with age
Lung collapse (rare)
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.
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
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.
American Academy of Family Physicians
The National Marfan Foundation
Canadian Family Physician
The Canadian Marfan Association
American Heart Association website. Available at: http://www.americanheart.org/presenter.jhtml?identifier=1200000 .
Mayo Foundation for Medical Education and Research website. Available at: http://www.mayo.edu .
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: http://www.niams.nih.gov/ .
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.