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.
Keywords: aortic dissection; ectopia lentis; fbn1 mutation; marfan syndrome; variant of unknown significance.
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