Marfan syndrome definition and facts* Marfan syndrome is a disease of connective tissues that is inherited. The severity of Marfan syndrome varies from one individual to another and it typically progresses over time. A tall, slender build is characteristic of Marfan syndrome..
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This website is all about the genetic disease Marfan Syndrome.
Marfan Syndrome isn't something that you can catch from someone, but it is something that parents can hand down to their children through genetics. It is also.
Genetic disease: Marfan syndrome is a genetic disease affecting the "connective tissue" in the body, with effects in various organ system. True Marfan syndrome is caused by a mutation in the fibrillin-1 gene, located on chromosome 15. Inheritance is autosomal dominant, and it appears that about 25 are spontaneous mutations..
The use of beta-blockers is needed to manage Marfan syndrome. If the aorta is affected, surgery will be needed. The people with Marfan syndrome should avoid the hard exercise. Check Also: 10 Facts about Malpractice. Facts about Marfan Syndrome 7: the rate. Marfan syndrome occurs on one of 3,,000 people in the world..