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Published on: May 21, 2017
Severe aortic root dilatation in infantile Marfan syndrome
Renita A Thomas1, Chikamuche T Anyanwu1, Maria Blazo1,2
1College of Medicine, Texas A&M University Health Science CenterBryanTexas.
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.
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