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- W2968165092 abstract "Cardiovascular manifestations of Marfan syndrome are associated with increased mortality, especially in the pediatric population. Early recognition is critical to long-term management. We present two cases of genetically defined classical Marfan syndrome presenting with severe infantile aortic root dilatation among siblings and discuss options for therapy." @default.
- W2968165092 created "2019-08-22" @default.
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- W2968165092 date "2019-08-12" @default.
- W2968165092 modified "2023-10-15" @default.
- W2968165092 title "Severe aortic root dilatation in infantile Marfan syndrome" @default.
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- W2968165092 doi "https://doi.org/10.1080/08998280.2019.1646594" @default.
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