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The risk for type B aortic dissection in Marfan syndrome
C Setacci1, G Galzerano, F Setacci
1Vascular and Endovascular Surgery Unit, Department of Medicine, Surgery and Neurological Sciences, University of Siena, Siena, Italy - setacci@unisi.it.
Abstract:
Marfan syndrome is the most prevalent connective tissue disorder, with an autosomal dominant inheritance with variable penetrance. This paper aims to summarize epidemiology and treatment for type B dissection in Marfan patients.
Insights
Marfan syndrome, a common connective tissue disorder, often involves type B aortic dissection. This review summarizes current knowledge on its epidemiology and treatment in affected patients.
Area of Science:
- Genetics and Medicine
- Cardiovascular Research
Background:
- Marfan syndrome is the most common inherited connective tissue disorder.
- It follows autosomal dominant inheritance with variable penetrance.
- Aortic dissection, particularly type B, is a serious complication.
Purpose of the Study:
- To summarize the epidemiology of type B aortic dissection in Marfan syndrome patients.
- To review current treatment strategies for type B aortic dissection in Marfan syndrome.
Main Methods:
- Literature review of epidemiological data.
- Analysis of treatment outcomes and guidelines.
Main Results:
- Epidemiological data on Marfan syndrome and type B dissection prevalence.
- Overview of medical and surgical management options.
- Discussion of risk factors and prognostic indicators.
Conclusions:
- Type B aortic dissection requires specialized management in Marfan syndrome.
- Multidisciplinary care is essential for optimal patient outcomes.
- Further research is needed to refine treatment protocols.
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