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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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| Publicado no: | Proc (Bayl Univ Med Cent) |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2019
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| Assuntos: | |
| Acesso em linha: | 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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