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Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report
Marfan’s syndrome is an autosomal dominant disorder of connective tissue characterized by a large number of possible mutations and by heterogeneity of clinical presentation primarily in skeletal, ocular and cardiovascular organ systems. Cardiovascular complications of the disease are responsible for...
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| 出版年: | SAGE Open Med Case Rep |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
SAGE Publications
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4857274/ https://ncbi.nlm.nih.gov/pubmed/27489631 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2050313X13507564 |
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