Marfan syndrome

Marfan syndrome is a genetic condition affecting the connective tissue. The disease is caused by dominant mutations in the fibrillin-1 gene. The condition affects the skeletal system, cardiovascular system, eyes, and skinIndividuals with the disease are typically very tall with long limbs.

Marfan Support & Information in NSW. 2009. About Marfan Syndrom. retrieved June 2, 2009 from http://images.google.ca/imgres?imgurl=http://www.marfan.net.au/images/human_body.jpg&imgrefurl=http://www.marfan.net.au/showcontent.toy%3Fcid%3D1515&usg=__l-z_XJED5dSuKGz5SXTRr033ohI=&h=364&w=520&sz=43&hl=en&start=18&um=1&tbnid=eR060Jafvqpq-M:&tbnh=92&tbnw=131&prev=/images%3Fq%3Ddefine:Marfan%2Bsyndrome%26hl%3Den%26sa%3DN%26um%3D1

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