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Ruptured abdominal aortic aneurysm repair in pediatric Marfan syndrome patient
Marfan syndrome is a well-described autosomal dominant connective tissue disorder with a constellation of anatomic characteristics including aortic degeneration as a result of the spontaneous mutation of the fibrillin gene, FBN1. Whereas life-threatening dissection and ascending aneurysmal rupture h...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849780/ https://www.ncbi.nlm.nih.gov/pubmed/29541693 http://dx.doi.org/10.1016/j.jvscit.2017.11.008 |