Is marfan's syndrome asociated with a shortened life span?

Yes. Marfan's syndrome patients die from complications of aortic valve widening. If this is treated with inderal, (propranolol) progression is slower and patients live longer. In addition, if heart valve surgey is performed electivelly patients live longer. Untrated patients have a life span of 32 years.
It depends . Patients with unrecognized marfan syndrome or patients with known marfan syndrome who do not receive appropriate medical care can have a shortened life span. The most typical threat to long life is aortic dissection and rupture. If appropriate surveillance for development of aortic aneurysm is performed, though, followed by heart surgery with significant aneurysm, lifespan can be long.

Related Questions

I have Marfan syndrome. Is there tests that can prolong my life expectancy?

Monitor issues. If you haven't done so yet, you should be followed at least on occasion by someone aware of the unique health issues of marfan patients. Surveillance of your heart & aortic root with cardiac ultrasound can pick up early signs of change that would warrant surgery. A thorough understanding of how the process has affected you may require a discussions with a geneticist. Read more...
An echocardiogram. If you have marfan syndrome, you should be aware that your cardiologist can use ultrasound to watch for the gradual enlargement of your aorta. Depending on your age, height, and weight, she can determine whether your aorta is growing larger than normal and recommend either medicine, like a beta blocker, or surgery to prevent dissection or rupture of the aorta. Read more...

For someone with Marfan syndrome. Is there treatments that can prolong his life expectancy?

Several treatments! Yes! children and adults with marfan syndrome can have gradual widening of the aorta - the major artery connected to your heart. Sometimes the aorta becomes so weak that it breaks. But your cardiologist can use an ultrasound machine to watch your aorta very carefully. She can treat you with medicines to slow down the enlargement, and your chest surgeon can even replace your aorta if necessary. Read more...
Yes. While there is no specific rx for this genetic connective tissue disorder, life is prolonged by treating it's complications. This reminds me of my patient i operated on for acute dissection of ascending aorta 26 years ago and 10 years later for enlarging abdominal aortic aneurysm. He is still alive today and i see him annually for check up. Read more...