Marfan syndrome is a genetic connective tissue disorder that is a frequent cause of aortic dissection in younger patients. We report a case of a patient with a history of ectopia lentis in his third decade and abdominal striae since adolescence, who presented with Stanford type A dissection at age 48.
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|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053542 | PMC |
| http://dx.doi.org/10.7759/cureus.23651 | DOI Listing |
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