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marfan syndrome is genetic disorder of connective tissue of the body. it cause a mutation of the gene that produces the protein fibrillin.
Yes, Marfan syndrome is a genetic disorder. It is not a disease. It is caused by a mutation in fibrillin and is an autosomal dominant mutation. This means that if you have a Marfan causing mutation, you have Marfan, and you have a 50/50 chance of passing it on to any children you may have. Severity of Marfan can vary within a family, even though all affected family members have the same mutation. It can not skip generations.
Yes Marfan syndrome is a dominate disorder that affects the bodies connective tissue. it also causes problems in the heart, eyes and bones
The genetic mutation responsible for Marfan was discovered in 1991.
Unfortunately no. The mutation that causes Marfan syndrome is found in every single cell in the body. It would be impossible to replace it in every cell.
Yes
It is caused by a mutation in the gene for fibrillin-1 on chromosone 15. A variable disorder of the connective tissue that effects many organ systems including the skeleton.eyes,heart,lungs and blood vessels.
It is a genetic disorder and if one parent has it, there is a 50?50 chance that the child will have it.
Anyone can get Marfans syndrome, it is a genetic disorder.
About 1 in 5,000 people have Marfan syndrome, including men and women of all races and ethnic groups. About 3 out of 4 people with Marfan syndrome inherit it, meaning they get the genetic mutation from a parent who has it. But some people with Marfan syndrome are the first in their family to have it; when this happens it is called a spontaneous mutation. There is a 50 percent chance that a person with Marfan syndrome will pass along the genetic mutation each time they have a child.
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
No, Marfan Syndrome is an inherited disorder of connective tissue. It is not an infectious disease.