Low visions ( weak eyes), Weak heart, weak artery, etc.
Marfan syndrome is found in 1 in every 5,000 - 10,000 births. If one of your parents has Marfan syndrome, you have a 50% chance of having Marfan 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.
Marfan Syndrome is a medical problem with the Conective Tissue.
Yes, Marfan syndrome is autosomal dominant.
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
A pregnant woman with Marfan should also receive genetic counseling regarding the 50% risk of having a child with the syndrome.
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
Marfan Syndrome is also known as Marfan's disease and hereditary connective tissue disorder. In some contexts, it may be referred to as Marfan syndrome type I or simply as a connective tissue disorder. However, the most common and widely recognized name remains Marfan Syndrome.
flat feet an sinked chest are some symptomes of marfan syndrome
They cant exercise as vigorously as someone without Marfan syndrome
Marfan syndrome is not naturally found in animals. However, researchers have created mice with Marfan syndrome in laboratories for the purpose of testing medications on them before conducting human trials.
The etiology of marfan syndrome would be the mutations in the protein FBN1 in the gene chromosome 15.