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Is marfan syndrome genetic?
yes
When can you get marfan syndrome?
Anyone can get Marfans syndrome, it is a genetic disorder.
What is a Marfan Syndrome?
marfan syndrome is genetic disorder of connective tissue of the body. it cause a mutation of the gene that produces the protein fibrillin.
When was the mutation responsible for Marfan syndrome discovered?
The genetic mutation responsible for Marfan was discovered in 1991.
Can Marfan Syndrome be detected before birth?
Yes, Marfan Syndrome can be detected before birth through prenatal genetic testing such as chorionic villus sampling or amniocentesis. These tests can detect whether the fetus has inherited the genetic mutation that causes Marfan Syndrome. It's important to consult with a genetic counselor or healthcare provider for further information and testing options.
How common is marfan syndrome?
Marfan's syndrome is the most common genetic disorder of connective tissue. It occurs in about every 10,000 to 20,000 individuals.
What has the author O V Lisichenko written?
O. V. Lisichenko has written: 'Sindrom Marfana' -- subject(s): Genetic aspects, Genetic aspects of Marfan syndrome, Marfan syndrome
What is marfansyndrome?
Marfan syndrome (also called Marfan's syndrome) is a genetic disorder of the connective tissue. People with Marfan's tend to be unusually tall, with long limbs and long, thin fingers.
Is Marfan's symdrome a transmitted disease?
Marfan's syndrome is a genetic disorder, so one would inherit it from their biological parents. You can't "catch" marfans syndrome
Does Marfan syndrome have a treatment?
While there is no cure for Marfan Syndrome (because it is a genetic disorder), there are ranges of treatment options can decrease (and even sometimes prevent) complications.
Is Marfan Syndrome common in a specific race?
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.
Are there any treatments for marfan syndrome?
While there is no cure for Marfan Syndrome (because it is a genetic disorder), there are ranges of treatment options can decrease (and even sometimes prevent) complications.
