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- W2997279690 abstract "Marfan syndrome is a connective tissue disorder caused by mutation in the FBN1 gene that results in a defect in the fibrillin-1 extracellular matrix protein. The primary cardiovascular complications include aortopathy and mitral valve disease.1 Some patients with Marfan syndrome have both pectus deformities and significant aortopathy, both of which may require surgical repair. Although concurrent surgical repair is more complex, the major advantage includes the lack of hemodynamic and respiratory compromise secondary to compression of thoracic organs postoperatively and has become more popular in recent years with excellent outcomes." @default.
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- W2997279690 date "2020-03-01" @default.
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- W2997279690 title "Combined pediatric heart transplant and Nuss procedure in a patient with Marfan syndrome" @default.
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- W2997279690 doi "https://doi.org/10.1016/j.xjtc.2019.11.002" @default.
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