Who discovered Marfan disorder?

In 1896 Dr. Antoine Marfan, a French paediatrician, first described what was later to be named “Marfan Syndrome” in a little girl that had very long fingers and limbs. Although Marfan syndrome was named after him because of his discovery, it was later found that the little girl suffered from another, related disease.

How was Marfan discovered?

In 1896, in the Bulletin of the Medical Society of Paris, Antoine Marfan described a five-year-old girl with arachnodactyly. It took almost 50 years to fully elucidate this syndrome including aneurysm of the ascending aorta.

What is Marfan syndrome named after?

As a result, many body systems are affected, including the heart, blood vessels, bones, tendons, cartilage, eyes, nervous system, skin and lungs. Named after Antoine Marfan, who first described the condition in 1896, the disorder is present at birth but may not be diagnosed until adolescence or young adulthood.

What does Marfan stand for?

Marfan syndrome is an inherited disorder that affects connective tissue — the fibers that support and anchor your organs and other structures in your body. Marfan syndrome most commonly affects the heart, eyes, blood vessels and skeleton.

What causes marfans?

Marfan syndrome is caused by a mutation in a gene called FBN1. The mutation limits the body’s ability to make proteins needed to build connective tissue. One in four people with Marfan syndrome develops the condition for unknown reasons. A person with Marfan syndrome has a 1 in 2 chance of passing it on to their child.

Can you play sports with Marfan syndrome?

The general guidelines for people with Marfan syndrome are to avoid competitive and contact sports that would put added stress on the aorta, cause chest or eye trauma, or be potentially damaging to loose ligaments and joints.