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- W1998513141 abstract "Marfan syndrome is an inherited, connective-tissue disorder transmitted as an autosomal dominant trait. Cardinal features of the disorder include tall stature, ectopia lentis, mitral valve prolapse, aortic root dilatation, and aortic dissection. Pectus excavatum may exist as an isolated lesion or in association with a genetic syndrome such as Marfan syndrome. We report the successful management of a simultaneous correction of pectus excavatum and the underlying cardiovascular diseases." @default.
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- W1998513141 date "2013-01-01" @default.
- W1998513141 modified "2023-09-23" @default.
- W1998513141 title "Combined Bentall and modified Ravitch procedures in a patient with Marfan syndrome" @default.
- W1998513141 doi "https://doi.org/10.4103/0970-9185.105812" @default.
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