As a result, the patient may develop various deformities of the skeleton or disorders related to the relative looseness of the ligaments.
About 90% of Marfan patients will develop cardiac complications.
Myopia (nearsightedness). Most patients with Marfan develop nearsightedness, usually in childhood.
People with Marfan syndome have problems with their eyes, heart, skeleton, and people with it are usually very tall and skinny
Between 50 and 80% of Marfan patients have dislocated lenses.
Marfan syndrome causes an increase in the length of the patient's bones, with decreased support from the ligaments that hold the bones together.
This condition is much more prevalent in patients with Marfan syndrome than in the general population.
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.
Marfan patients may develop kyphosis either in the upper (thoracic) spine or the lower (lumbar) spine.
In patients with Marfan, it is the abnormal mitral valve that is most likely to become infected.
Yes, Marfan syndrome is autosomal dominant.
Marfan Syndrome is a medical problem with the Conective Tissue.
Some patients with Marfan develop cystic disease of the lungs or recurrent spontaneous pneumothorax, which is a condition in which air accumulates in the space around the lungs. Many will also eventually develop emphysema.