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A rare cause of recurrent aortic dissection
We report the case of a 19-year-old man with a history of Loeys–Dietz syndrome (LDS), which was diagnosed when he had a Stanford type A aortic dissection. He also had multiple aneurysms including ones in the innominate, right common carotid, and right internal mammary arteries. He had had multiple p...
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| Udgivet i: | J Saudi Heart Assoc |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Elsevier
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4917711/ https://ncbi.nlm.nih.gov/pubmed/27358537 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jsha.2015.11.005 |
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