Clinical management and maternal-fetal outcomes of a patient with an atypical mutation in the FBN-1 gene suggestive of Marfan syndrome: A case report
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Abstract
Marfan syndrome (MFS) is an autosomal dominant connective tissue disease that is often accompanied by heart valve abnormalities and aortic aneurysms. It is usually associated with a mutation in the FBN-1 gene. Pregnancy is generally contraindicated in patients with MFS. In this report, we present the case of a pregnant woman
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- europepmc
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