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Risk Prevalence is estimated at 1:5000 people. Inherited as autosomal dominant trait, though 25% of cases are sporadic. The 2010 Ghent Nosology for Marfan Syndrome guides Dx, heavily prioritizing aortic root dilation, ectopia lentis, and family history. Perioperative Risks Aortic…
Introduction Historical Notes on Thoracic Aortic Aneurysms The dilatation of arteries was first recognized as a disease of the cardiovascular system in Egypt in the 1550s bc , and the first to describe an abdominal aortic aneurysm was the Flemish…