Do you have any information about this syndrome? I would like to know more.
The condition usually has one in every 1 person, but it can be said to be between 1 and 2. There are currently thousands of patients with Marfan syndrome in the United States. It can occur both in children and in adults and in men and women. This disorder has been present since birth and is sometimes detectable in infants. However, its symptoms sometimes do not appear until adolescence or adolescence, and the severity of symptoms varies widely. Its prevalence is equal in men and women.
It is a genetic disorder. This abnormality is due to mutations in chromosome 3. The function of this gene is to express the instructions for making fibrillin. Marfan syndrome is a type of hereditary disorder that primarily targets the connective tissue of the body, and patients with this syndrome have longer bones and muscles more relaxed than normal. There are many disorders in their eyes and cardiovascular system.