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 ...

ACCORDING to the Marfan Association around 10,000 people in the UK suffer from Marfan syndrome. But what do we know about the hereditary condition, and what are the symptoms? What is Marfan syndrom… ...

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 ...

Alternatively, in approximately 25-30% of those with Marfan syndrome the condition has developed due to a spontaneous mutation yielding the defective gene. Marfan syndrome occurs in approximately ...

A rare disease, Marfan Syndrome can cause sudden cardiac death in the young and in athletes, but Marfan is only one disease that kills young athletes. "Reasonable and careful screening of young ...

It was later revealed that Larson had Marfan Syndrome. The genetic disorder is found in approximately 50,000 Americans today, or one in 5,000 to 10,000 people, experts estimate.

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 cure.

Connective tissue holds all the body’s cells, organs and tissues together, according to The Marfan Foundation. The syndrome, which weakens the tissue, is caused by a defect (or mutation) in the ...

About 3 out of 4 people with Marfan syndrome inherit it, meaning they get the genetic mutation from a parent who has it. Marfan syndrome is a connective tissue disorder that affects 1 in 5,000 people.

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 ...

Learn the symptoms of Marfan syndrome. ... Marfan syndrome is caused by a genetic mutation that leaves connective tissue in the body weak, according to the National Institutes of Health.