marfan syndrome life expectancy reddit
An aortic aneurysm can be life threatening. I have Marfan syndrome a genetic disorder that affects the bodys connective tissue.
Marfan Syndrome Circulation Cardiovascular Genetics
Family members have passed on from Marfans related deaths at the age of 29 39 42 43 60 and 65.
. The median cumulative probability of survival was 61 years significantly increased compared with the median survival. The life expectancy in this syndrome has. Nowadays people with Marfan syndrome live until age 70 which is comparable to the average life expectancy of the general population.
Long thin hands and feet. An aortic aneurysm can cause the walls of the aorta to tear apart dissect and blood to leak in the space created by the tear. And a specific pattern of language and learning disabilities.
A newly recognized syndrome of Marfanoid habitus. 3540 years is the average for someone who doesnt follow guidelines such as not exercising riding. The biggest risk is an enlarged aorta the major artery taking blood away from the heart.
The figure of 30 years is somewhat old and was. Its easy to go. People who are properly diagnosed adapt their lifestyle and receive appropriate medical and surgical management can live a normal life span into the 70s.
One in 10 patients may have a high risk of death with this syndrome due to. In around three-quarters 75 of cases Marfan syndrome is inherited from 1 parent. Median estimate male.
I play recreational basketball sail and ride a bicycle. 708752 The median cumulative probability of aortic event-free survival. Despite the high risk for Marfan related cardiovascular problems the average life expectancy of those with Marfan syndrome is nearly 70 years.
The average age at death for the 72 deceased patients was 32 years. 73 years 95 CI. Marfan syndrome is hereditary which means it can be passed to a child from a parent whos affected.
There is a 50 percent chance that a person with Marfan. Now at the age of 27 I am married I have an amazing family most of whom have Marfan syndrome as well and I have traveled the world with my husband and some of my. But some people with Marfan syndrome are the first in their family to have it.
When this happens it is called a spontaneous mutation. I am 38 right now and happy to be here. I had a 2D echocardiogram done to see if my aortic root is larger than normal and luckily its not.
There is no cure for Marfan syndrome but life expectancy has increased significantly over the last few decades when and is now similar to that of the average person. Life expectancy for my family members with Marfans hasnt been great but there is a range. The leading cause of death in Marfan syndrome is heart disease.
The Mighty teamed up with The Marfan Foundation to ask their community what they wished others understood about Marfan syndrome. With proper treatment they can live up to half the time a normal person would or longer. This poor survival was demonstrated in a series of 257 patients with the Marfan syndrome.
Both children and adults can live Marfan syndrome as. 63 years 95 CI. Average life expectancy - 60 years.
The survival of untreated patients with Marfan syndrome is reduced by about one third with death occurring at an average age of 30-40 years. Cardiac problems led to 52 of. The average life expectancy of those affected by Marfans is about 70.
Hey everyone for context I have basically every single physical symptom of marfans besides visual difficulties. The average age of death was 32. Posting this as a separate comment because I just looked it up.
The thought of an early death does scare worry. Heres what they had to say. Thats the killer in Marfans the aortic root swells up to three times the normal size and blood has a possibility of going backwards in the heart causing death.
Survival curves were generated and data were analyzed. I had a chance to be part of the study but i opted out because my aorta reached 5cm dilation so my cardiologist said it was time for surgery. Back when I was 16 I had an echo done which said my aortic root was 256.
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