Multidisciplinary approach to a Marfan syndrom patient with emphasis on cardiovascular complications

Abstract

Background. Marfan syndrome (MFS) is the most common inherited disorder of connective tissue affecting multiple organ systems. Most life-threatening and life-shortening complication is aortic dissection. Without surgery, life expectancy of MFS patients is reduced to approximately 32 years. Early identification and appropriate multidisciplinary medical cooperation is essential. Conclusion. Proper follow up, therapy and timely surgical repair lead to almost regular lifespan of affected individuals.