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What percentage of Marfan syndrome sufferers eventually develop cardiac complications?
About 90% of Marfan patients will develop cardiac complications.
How many Marfan syndrome sufferers develop ectopia lentis?
Between 50 and 80% of Marfan patients have dislocated lenses.
What is the racial breakdown of Marfan syndrome sufferers?
Marfan syndrome affects males and females equally, and appears to be distributed equally among all races and ethnic groups.
Why do Marfan syndrome sufferers develop longer bones?
Marfan syndrome causes an increase in the length of the patient's bones, with decreased support from the ligaments that hold the bones together.
Why should Marfan syndrome sufferers never smoke?
Smoking is particularly harmful for Marfan patients because it increases their risk of emphysema.
What part of the heart is most likely to develop infection in Marfan syndrome sufferers?
In patients with Marfan, it is the abnormal mitral valve that is most likely to become infected.
What treatment is recommended for Marfan syndrome sufferers?
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.
How does pectus carinatum impact Marfan syndrome sufferers?
Although pectus carinatum does not cause breathing difficulties, it can cause embarassment about appearance.
What are the chances of getting marfan syndrome?
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.
Is marfan syndrome automsomal dominant?
Yes, Marfan syndrome is autosomal dominant.
What does Marfan syndrome mean?
Marfan Syndrome is a medical problem with the Conective Tissue.
Is Marfan syndrome contagious?
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
