People affected with Marfan's typically have long bones that are longer than normal (i.e. longer than normal legs and arms), longer than normal fingers, joints that are naturally more flexible than the average person. They can also have problems with their heart, aortic artery, and eyes.
flat feet an sinked chest are some symptomes of marfan syndrome
people with marfan syndrome are typically very tall with loose jointed. people with marfan disease usually have long narrow faces.
The symptoms of Marfan syndrome in some patients resemble the symptoms of homocystinuria, which is an inherited disorder marked by extremely high levels of homocystine in the patient's blood and urine.
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
When you are born, because it's genetic.
The treatment and management of Marfan is tailored to the specific symptoms of each patient. Some patients find that the syndrome has little impact on their overall lifestyle; others have found their lives centered on the disorder.
People with Marfan syndome have problems with their eyes, heart, skeleton, and people with it are usually very tall and skinny
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.
Yes, Marfan syndrome is autosomal dominant.
Marfan Syndrome is a medical problem with the Conective Tissue.
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
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.