Combined Bentall and modified Ravitch procedures in a patient with Marfan syndrome

Combined Bentall and modified Ravitch procedures in a patient with Marfan syndrome

Marfan syndrome is an inherited, connective-tissue disorder transmitted as an autosomal dominant trait. Cardinal features of the disorder include tall stature, ectopia lentis, mitral valve prolapse, aortic root dilatation, and aortic dissection. Pectus excavatum may exist as an isolated lesion or in...

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Bibliographic Details
Main Authors: Bhuvnesh Kansara, Ajmer Singh, Samir Girotra, K S Iyer
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Journal of Anaesthesiology Clinical Pharmacology
Subjects:
Aortic aneurysm
Marfan syndrome
pectus excavatum
Online Access:http://www.joacp.org/article.asp?issn=0970-9185;year=2013;volume=29;issue=1;spage=95;epage=98;aulast=Kansara

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http://www.joacp.org/article.asp?issn=0970-9185;year=2013;volume=29;issue=1;spage=95;epage=98;aulast=Kansara

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