marfan syndrome life expectancy reddit

As early as the 1970s the life expectancy of people with Marfan syndrome was projected as at least two-thirds of a person without the disease. The most serious complications involve the heart and aorta with an increased risk of mitral valve prolapse and aortic aneurysm.


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The life expectancy in this syndrome has increased to greater than 25 since 1972.

. Those with the condition tend to be tall and thin with long arms legs fingers and toes. 19k Members 9 Online Created Mar 24 2011 rmarfans Rules 1. After a follow-up of 38 months they concluded that elevated TGF-β levels correlate with 1 larger aortic root diameters 2 faster aortic root growth and 3 earlier aortic root surgery when TGF-β1 level is 140 pgmL.

As a result a new group of adult patients with congenital cardiac defects requires medical rehabilitation. Cardiac problems led to 52 of the 56 deaths of known cause with aortic dilatation and. Management by expert centres extends the life expectancy of Marfan patients to over 60 years of age.

This thread is archived. Long arms legs and fingers - most of us tall people have those. Nowadays people with Marfan syndrome live until age 70 which is comparable to the average life expectancy of the general population.

Advances in medical interventional and surgical treatment have increased average life expectancy of patients with congenital heart defects. Most people who have Marfan syndrome or a related condition are able to lead productive and satisfying lives thanks to advances in medical treatment that have greatly extended life expectancy. Marfan syndrome is a heritable disorder of the connective tissue with an estimated prevalence of 1 in 5000 individuals and no predilection for either sex.

The average age at death for the 72 deceased patients was 32 years. There is a 50 percent chance that a person with Marfan syndrome will pass along the genetic mutation each time they have a child. Having Marfan syndrome does not mean patients might not acquire other conditions that are common in the aging population.

This is a subreddit for people living with Marfan Syndrome to come together and ask questions discuss issues and provide support. In 20142015 16 were deceased 47 of 68 survivors consented to new clinical investigations. 64 193 cm 1134 smoots AZ.

Tall and thin body type - ditto. Despite the high risk for Marfan related cardiovascular problems the average life expectancy of those with Marfan syndrome is nearly 70 years. People who are properly diagnosed adapt their lifestyle and receive appropriate medical and surgical management can live a normal life span into the 70s.

But some people with Marfan syndrome are the first in their family to have it. New comments cannot be. What is my life expectancy with marfans syndrome.

There are a number of potential indicators of marfans. Different people exhibit different ones. People who are accurately diagnosed adapt proper lifestyles and receive appropriate medical and surgical management may live for a normal life span into their 70s.

I know they say life expectancy for those with Marfans is similar to the general population so long as you seek proper medical care take your medicine etc. However there are no guarantees and having Marfan syndrome does not mean you might not acquire other conditions that are common in the aging population. 1 Such centres usually have a generalist with broad experience with Marfan patients to.

Curved spine - You dont seem to exhibit this one. However there are no guarantees. Day-to-day management including routine treatment and attention to physical activity guidelines is a powerful way to safeguard your health and.

When this happens it is called a spontaneous mutation. Franken et al 26 analyzed 99 patients with MF syndrome carrying an FBN1 mutation. Do not give medical advice Moderators Moderator list hidden.

Marfan syndrome MFS is a rare multi-systemic genetic disorder that affects the connective tissue. The syndrome is associated with classic ocular cardiovascular and musculoskeletal abnormalities although involvement of the lung skin and central nervous system may also occur67 Decreased life expectancy occurs primarily due to aortic complications including aortic root dilatation and dissection8. MFS is a heritable connective tissue disorder associated with reduced life expectancyprimarily due to aortic pathology.

No requests for Medical Advice including diagnosis. They also typically have overly-flexible joints and scoliosis. The median cumulative probability of survival was 61 years significantly increased compared with the median survival of 47 years for patients with Marfan syndrome determined 30.

Marfan syndrome is a serious potentially life-threatening condition and an. Methods A followup study of 84 MFS adults initially investigated in 20032004. Patients with Marfan syndrome MFS are a relevant group among these patients.

One in 10 patients may have a high risk of death with this syndrome due to heart problems.


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