Pathophysiology of Marfan Syndrome
Автор: A & P Live Studio
Загружено: 2026-03-15
Просмотров: 2
Описание:
Marfan syndrome is a genetic connective tissue disorder diagnosed using the revised Ghent criteria and managed through a combination of medical and surgical interventions. Current guidelines recommend medications such as beta-blockers and angiotensin receptor blockers to slow aortic dilation, while valve-sparing root replacement is increasingly preferred over traditional grafts to avoid lifelong blood thinners. Multidisciplinary care and shared decision-making remain central to optimizing patient outcomes and managing the severe cardiovascular risks associated with the disease.
What is the revised Ghent nosology for Marfan syndrome?
How do Multidisciplinary Aortic Teams improve patient survival?
What are the surgical thresholds for bicuspid aortic valves?
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