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...

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Detalles Bibliográficos
Autores principales: Lu, Joyce J., Slaikeu, Jason D., Wong, Peter Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Aortic aneurysm and dissection
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

Internet

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

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