. "Marfan syndrome (MFS) is the most common inherited disorder of connective tissue affecting multiple organ systems. The 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 an almost normal lifespan in affected individuals." . . "1"^^ . "cardiovascular complications; aortic dissection; aorta; aneurysms; Marfan syndrome"@en . "157" . "http://biomed.papers.upol.cz/pdfs/bio/2013/01/01.pdf" . "RIV/61989592:15110/13:33144464!RIV14-MSM-15110___" . . . "1"^^ . "CZ - \u010Cesk\u00E1 republika" . . "RIV/61989592:15110/13:33144464" . . "Multidisciplinary approach to a Marfan syndrome patient with emphasis on cardiovascular complications."@en . "I" . "[95FD7C69813D]" . . . "Multidisciplinary approach to a Marfan syndrome patient with emphasis on cardiovascular complications."@en . "Multidisciplinary approach to a Marfan syndrome patient with emphasis on cardiovascular complications." . "1" . . "90033" . "4"^^ . . "1213-8118" . . "\u0160antav\u00FD, Petr" . "Multidisciplinary approach to a Marfan syndrome patient with emphasis on cardiovascular complications." . . . "Marfan syndrome (MFS) is the most common inherited disorder of connective tissue affecting multiple organ systems. The 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 an almost normal lifespan in affected individuals."@en . . "10.5507/bp.2013.023" . "Biomedical Papers-Olomouc" . . . "15110" . .