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Paper Information

Journal:   IRANIAN HEART JOURNAL (IHJ)   SPRING 2012 , Volume 13 , Number 1; Page(s) 55 To 58.
 
Paper: 

AORTIC SURGERY IN A PATIENT WITH MARFAN SYNDROME AND PECTUS EXCAVATUM

 
 
Author(s):  BAGHAEI R., NOOHI F.*, TOOTOONCHI Z., MOHEBBI B., AZARSHAB A.
 
* RAJAIE CARDIOVASCULAR, MEDICAL AND RESEARCH CENTER, TEHRAN UNIVERSITY OF MEDICAL SCIENCES
 
Abstract: 
Severe cardiovascular disorders, including aortic dissection and aneurismal dilation of the aorta, are the main life-threatening complications of the Marfan syndrome 1. Approximately two thirds of individuals who have this syndrome have chest wall deformities such as pectus excavatum or pectus carinatum 2. When a patient with pectus excavatum needs aortic surgery, the surgeon may face a major clinical challenge in choosing the optimal surgical approach 3. We present a case of the Marfan syndrome with severe pectus excavatum who underwent aortic surgery.
 
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