Marfan Syndrome

Marfan syndrome is a rare, inherited disorder of connective tissue and growth. The disease affects several parts of the body.

The disease is highly variable, which means that different people with the condition will have different parts of their body affected to a greater or lesser degree.

The features of Marfan syndrome result from changes in the body's connective tissue and in the control of body growth. Connective tissue holds our bodies together. It is found throughout the body, which is why it can affect many different parts of the body.

Marfan syndrome most commonly affects the heart and blood vessels, the bones and joints and the eyes. It can also affect the lungs and the skin. The number and type of features that are present can vary a lot between different people with Marfan syndrome. Some will have only a few features, while others will have many.

At UCSF, a team of experts can help identify signs and symptoms of Marfan syndrome, diagnose the disease and find the best treatment plan for patients.

To make an appointment or to get more information about the UCSF Program in Cardiovascular Genetics, please call (415) 476-5354.

For help finding a doctor, contact our Physician Referral Service:

Reviewed by health care specialists at UCSF Medical Center.
Last updated November 18, 2008