Marfan syndrome is a rare genetic problem that affects the body’s connective tissue. Connective tissue supports and connects many of the body's structures. Marfan syndrome affects many systems in the body, such as the:
Interior of Heart
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This problem is caused by a faulty gene. It is inherited from a parent.
This problem is more common in people who have family members with Marfan syndrome.
Problems range from mild to severe. It can affect one or many parts of the body. Some symptoms may happen at an early age. Others may happen later in life or worsen with age.
The problems a person will have depend on the parts of the body affected by Marfan syndrome. Some problems may be:
The doctor will ask about your symptoms and health history. You may also be asked about your family's medical history. A physical exam will be done. An eye exam may also be done. Marfan syndrome is hard to diagnose.
Heart function may be tested. This can be done with an echocardiogram.
Images of the body may be taken. This can be done with:
There is no cure. A person will need lifelong monitoring.
The goal of treatment is to manage symptoms. Choices are:
Some people may need braces or surgery.
Exercise and medicine may be needed to ease back pain.
There are no guidelines to prevent this health problem.
Family Doctor—American Academy of Family Physicians
National Marfan Foundation
Canadian Marfan Association
College of Family Physicians of Canada
Marfan syndrome. EBSCO DynaMed website. Available at: https://www.dynamed.com/condition/marfan-syndrome. Accessed February 8, 2021.
Pepe G, Giusti B, et alS. Marfan syndrome: current perspectives. Appl Clin Genet. 2016 May 9;9:55-65.
What is Marfan syndrome? National Marfan Foundation website. Available at:
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Accessed February 8, 2021.
Last reviewed December 2020 by EBSCO Medical Review Board
James P. Cornell, MD
Last Updated: 2/8/2021