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Severe aortic root dilatation in infantile Marfan syndrome
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 roo...
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| Publié dans: | Proc (Bayl Univ Med Cent) |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Taylor & Francis
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6793975/ https://ncbi.nlm.nih.gov/pubmed/31656420 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/08998280.2019.1646594 |
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