Entscheidungen über die Planung einer Familie können schwierig und emotional sein, wenn eines der zukünftigen Elternteile eine genetische Erkrankung wie das Marfan-Syndrom hat. Bevor eine Entscheidung getroffen wird, sollten sich Eltern über die vielen Möglichkeiten informieren, die heutzutage zur Verfügung stehen, sowie über die möglichen Risiken für Mutter und Kind. Ein genetischer Berater oder die medizinische Fachkraft im Help & Resource Center der Marfan Foundation kann Ihnen Informationen geben und Ihre Optionen mit Ihnen besprechen.
Related Resources
MASS Phenotype
MASS Phenotype is a connective tissue disorder that is similar to Marfan syndrome in that people with the condition have the similar Mitral valve, Aorta, Skin, and Skeletal features. People with MASS phenotype do not have lens dislocation, but rather myopia (nearsightedness), and do not show progressive and dangerous aortic root enlargement, hallmark features of Marfan syndrome. What other […]
Endocarditis Prophylaxis for People with Marfan Syndrome
Endocarditis Prophylaxis for People with Marfan Syndrome In April 2007, the American Heart Association (AHA) revised its guidelines for antibiotic treatment at the time of dental procedures and other medical situations in which there is a high likelihood of bacteria entering the bloodstream. In general, the AHA guidelines are the “gold standard” in the United […]
Teens and Marfan Syndrome
If you were recently diagnosed with Marfan syndrome or if you have known about it for years, there are probably hundreds of thoughts, questions, and concerns rushing through your head. On one hand, there is a whole new world of medical information to learn. On the other hand, there is your life as a teen. […]
Know the signs.
Fight for victory.
Join us in the fight for victory over Marfan syndrome and related conditions and help us create a brighter future for everyone living with these conditions.