What is Marfan syndrome?

Marfan syndrome is a genetic disorder that affects the body’s connective tissue. Connective tissue protects, supports, and gives structure to all other tissues and organs in the body. This condition most often affects the heart, blood vessels, eyes, bones, and spine. It can range from mild to serious.

Doctors in different specialties treat Marfan syndrome, including heart and vascular experts, ophthalmologists, and orthopaedists, among others. At Penn Medicine, our expert clinicians work collaboratively across disciplines, offering a comprehensive approach to care that treats your symptoms and helps you stay healthy.

Marfan syndrome symptoms

The symptoms of Marfan syndrome can vary widely, even among members of the same family. Some people have features and symptoms early in life, but others don’t develop any signs until adulthood. The effects of Marfan syndrome may worsen over time. They can be life-threatening, depending on what parts of the body are affected.

People with Marfan often have:

  • Arms, legs, fingers, and toes that are longer than expected
  • Taller stature than expected for the family
  • Breastbone that sticks out or in (pectus exacavtum or carinatum)
  • Crowded teeth
  • Curved spine (scoliosis)
  • Flat feet
  • Heart murmurs, floppiness of the mitral valve (mitral valve prolapse), or widening of the aorta where it leaves the heart
  • Nearsightedness
  • Stretch marks on the skin that weren’t caused by pregnancy or fluctuations in weight

What causes Marfan syndrome?

Marfan syndrome is caused by a change in a gene (a variant) that affects a protein needed to make tissues strong and elastic. It often involves a variation in the FBN1 gene.

Most people with Marfan syndrome inherit it, when it’s passed down from parent to child. Though sometimes the condition occurs spontaneously with no prior history in the family. If you’ve inherited Marfan syndrome, genetic testing and counseling can help you understand what this might mean to you and your family.

How is Marfan syndrome diagnosed?

Because Marfan syndrome can be a serious, even life-threatening condition, early diagnosis is critical. Your doctor will ask you detailed questions about your health background and family medical history, then do a thorough physical exam to look for features of Marfan syndrome. They’ll often recommend genetic tests, along with an eye exam, imaging scans, and heart tests to confirm a diagnosis.

CT scan
A CT scan helps diagnose traumatic injuries, cancer, vascular diseases, and many other conditions.
Echocardiogram
An echocardiogram is a test that uses sound waves to create pictures of the heart. The picture and information it produces is more detailed than a standard x-ray image. An echocardiogram does not expose you to radiation. x-ray
Electrocardiogram
An electrocardiogram (ECG) is a test that records the electrical activity of the heart.
MRI
An MRI provides high-resolution images of the brain, spine, and many other structures in the body.

Ways to treat Marfan Syndrome

There’s no cure for Marfan syndrome, but treatment can help you live a long and full life. Regular checkups with eye exams and imaging tests of the heart and spine are often used to monitor your condition over time and catch any issues early. Certain medications and genetic counseling may also be recommended. Advanced cases may require cardiac, orthopaedic, or eye surgery.

Aorta surgery
These complex procedures repair or replace damaged sections of the aorta, the body’s largest artery.
Aortic valve repair and replacement surgery
Our specialists perform both open and minimally invasive surgery to fix or replace impaired aortic valves.
Cataract surgery
This treatment removes a cloudy lens caused by cataracts and replaces it with a clear artificial one.
Glaucoma surgery
When eye drops and laser procedures don’t lower eye pressure, this glaucoma treatment is the next step.
Spinal fusion
This surgical procedure joins bones in the spine using bone grafts, metal plates, screws, or rods.

Specialized care for your whole body

Marfan syndrome can affect many different areas of your body from your heart to your spine to your eyes. At Penn Medicine, you’ll have access to experts in a wide range of disciplines who work together to create an individualized care plan tailored to your needs.

This includes medical genetics teams with experience in inherited cardiac disease and clinicians at Penn Medicine’s Aorta Center, which provides advanced cardiac treatment for those who need it. Our opthalmologists and orthopaedic specialists are key collaborators too, making it possible for you to receive well-rounded care in one encompassing health system.

Related specialties

Center for Inherited Cardiovascular Disease
Inherited heart disease covers many genetic heart conditions that affect multiple generations.
Genetic counseling
Our experienced genetic counselors offer testing options and help you understand results.
Ophthalmology
Our expert eye care is focused on protecting your vision and supporting lifelong eye health.

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