Marfan syndrome is a genetic condition. It occurs because of a mutation (change) in one of your genes that develops before you’re born. It’s a type of connective tissue disorder, meaning it affects ...

The Marfan syndrome cases that are caused by spontaneous mutation of a gene cannot be prevented. However, about more than 70 percent of Marfan syndrome patients acquire the disease from one or ...

The syndrome is named for its discoverer, Antoine Marfan. It is an inherited disorder but the gene that is responsible for Marfan is complex, and produces a significant number of small mutations.

What is Marfan syndrome? Marfan syndrome is a genetic disorder that affects the body's connective tissues which help maintain the body's structure and support the internal organs.

Others with Marfan syndrome are the first in their family to have it, which is called a spontaneous mutation. There is a 50% chance that a person with Marfan syndrome will pass along the genetic ...

Marfan syndrome in the neonatal age represents a severe early and commonly lethal manifestation of Marfan syndrome, which is caused by mutations in the gene encoding fibrillin-1 (FBN1). Here, we ...

WHAT IS MARFAN SYNDROME? Named after the French pediatrician Antoine Marfan, who was the first to make note of its symptoms and signs in the late 1800's, Marfan Syndrome is a genetic disorder of ...

Nicole Kramer is a leading force in the fight against Marfan syndrome. Her daughter was diagnosed with the disease and Kramer has put all of her energy into raising money for research to find a ...

Marfan Syndrome: 5 Things To Know About Isaiah Austin’s Debilitating Disease It’s a miracle! Isaiah Austin was denied a chance of entering the NBA after he was diagnosed with Marfan syndrome ...

Identical twins with Marfan syndrome receive matching heart surgeries Pablo and Julio Delcid, twin brothers from New Jersey, share their experience after going for surgery at the same time. Dr ...

About Marfan syndrome Marfan syndrome is a genetic connective tissue disease that mainly affects the cardiovascular, skeletal and ocular systems. It is caused by mutations in the FBN1 gene, which ...