Marfan syndrome has been around since Ernesto and Shampoo Money started dating. They had a child who had a child who had a child who had a cousin who had a cousin and that cousin had a child and the child had a friend who knew a guy who knew a guy that had marfans syndrome.
There is a 100% probability of his child having Marfan's syndrome. The syndrome is carried by the FBN1 gene, and is dominant so there is no way to avoid having the disease. However the severity of it may vary from mild to severe, so his child may suffer from a mild form of the syndrome.
A pregnant woman with Marfan should also receive genetic counseling regarding the 50% risk of having a child with the syndrome.
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.
How Common Is Marfan Syndrome?According to the National Marfan Foundation - Marfan.org - 1 in every 5,000-7,000 babies born is a child with Marfan syndrome. Other statistics about Marfan syndrome75% of people with Marfan syndrome have an affected parent.Approximately 25% of all cases are due to de novo(spontaneous) genetic mutations. This means they are the first person in their family to be affected.Marfan syndrome is an autosomal dominant mutation; this means that, if the mutation is present, the person has the syndrome to at least a mild degree. It can not skip generations. A person with Marfan has a 50% chance of passing it on to their children.Estimates indicate that approximately 0.02% of the global population has Marfan syndrome.Marfan syndrome is found equally in all ethnicities.
One can find information on marfan on its official website. Marfan syndrome is a disorder that affects connective tissue. It is usually passed from parent to child through genes.
It is a genetic disorder and if one parent has it, there is a 50?50 chance that the child will have it.
There is a 50% chance that the baby will have Marfan. The father might pass on the gene that has the Marfan mutation, or he might pass on the gene that does not. Each child you have together has a 50% chance.
Marfan syndrome can affect learning abilities if a child experiences vision problems, attention deficits, or learning disabilities associated with the condition. However, with appropriate support and accommodations, individuals with Marfan syndrome can still achieve academic success. Regular monitoring and early intervention can help address any learning challenges that may arise.
Pleiotropy.
In addition, a child with undiagnosed nearsightedness related to Marfan may have difficulty seeing the blackboard or reading printed materials, and thus do poorly in school.
Have a 50% chance of passing it on to there offspring. This is called an autosomal dominant gene. What that means is, considering each human has TWO sets of chromosomes (1 from mom, 1 from dad), it takes only ONE copy of the mutated gene being passed on for the child to inherit the syndrome. Because for the conception of each child there is a chance of passing one or the other gene on, there is a 1 in 2 or 50% chance of giving the child Marfan Syndrome.