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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...
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| Vydáno v: | J Vasc Surg Cases Innov Tech |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5849780/ https://ncbi.nlm.nih.gov/pubmed/29541693 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jvscit.2017.11.008 |
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