marfan syndrome life expectancy reddit

What is my life expectancy with marfans syndrome. Created Mar 24 2011.


Neonatal Marfan Syndrome Signs Of Marfan In A Newborn

The average age at death for the 72 deceased patients was 32 years.

. I was wondering if anyone on the science sub here had insight on it. Hints and such dont work especially for big decisions. Cardiac problems led to 52 of.

Five and 10 year survival after diagnosis was 95 and 88 and the five and 10 year complication free survival was 78 and 66 respectively. Both children and adults can live Marfan syndrome as. Marfan syndrome MFS is a pleiotropic connective tissue disease inherited as an autosomal dominant trait due to mutations in the FBN1 gene encoding fibrillin 1.

Usually very tall skinny long fingers. This thread is archived. This poor survival was demonstrated in a series of 257 patients with the Marfan syndrome.

Ive been told I have it by some doctors but it doesnt really bother me. There were 45 deaths representing. Marfan syndrome can cause dislocation of the lens of the eye and.

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. First of all if you want to have a lasting relationship you need to be completely open with each other communication-wise. A total of 206 patients with Marfan syndrome were ascertained throughout genetic clinics in Wales and Scotland during the period 19701990.

Most people with Marfan. Compared with the population with Marfan syndrome studied by Murdoch et al life expectancy is prolonged by 14 years. My theory is the increased protein and reduced cardiovascular strain would probably increase life expectancy but Im.

Anyone here have it. The life expectancy in this syndrome has increased to greater than 25 since 1972. There were 45 deaths representing.

Im curious how much truth. Marfan syndrome is caused by a defect in the gene that enables your body to produce a protein that helps give connective tissue its elasticity and strength. The Marfan syndrome is an autosomal dominant disorder of the connective tissue with mutations on the fibrillin-1 gene encoding for fibrillin a major component of the extracellular microfibrils.

New comments cannot be posted and votes. Marfan syndrome is inherited as an autosomal dominant genetic disease. The survival curve of the Murdoch population differs.

Marfan syndrome affects the skeleton eyes heart and blood vessels nervous system skin and respiratory system. A total of 206 patients with Marfan syndrome were ascertained throughout genetic clinics in Wales and Scotland during the period 19701990. Nowadays people with Marfan syndrome live until age 70 which is comparable to the average life expectancy of the general population.

Marfan syndrome is a genetic. Something that can effect us tall folks is Marfan Syndrome. This is a subreddit for people living with Marfan Syndrome to come together and ask questions discuss issues and provide support.

That means that if someone has Marfan syndrome they have a 50 chance that their child will get. Advances in the management of the cardiovascular manifestations of this syndrome have led. Despite the high risk for Marfan related cardiovascular problems the average life expectancy of those with Marfan syndrome is nearly 70 years.


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