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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Main Authors: Bhuvnesh Kansara (Author), Ajmer Singh (Author), Samir Girotra (Author), K S Iyer (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2013-01-01T00:00:00Z.
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MARC

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042 |a dc 
100 1 0 |a Bhuvnesh Kansara  |e author 
700 1 0 |a Ajmer Singh  |e author 
700 1 0 |a Samir Girotra  |e author 
700 1 0 |a K S Iyer  |e author 
245 0 0 |a Combined Bentall and modified Ravitch procedures in a patient with Marfan syndrome 
260 |b Wolters Kluwer Medknow Publications,   |c 2013-01-01T00:00:00Z. 
500 |a 0970-9185 
500 |a 10.4103/0970-9185.105812 
520 |a 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 association with a genetic syndrome such as Marfan syndrome. We report the successful management of a simultaneous correction of pectus excavatum and the underlying cardiovascular diseases. 
546 |a EN 
690 |a Aortic aneurysm 
690 |a Marfan syndrome 
690 |a pectus excavatum 
690 |a Anesthesiology 
690 |a RD78.3-87.3 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Journal of Anaesthesiology Clinical Pharmacology, Vol 29, Iss 1, Pp 95-98 (2013) 
787 0 |n http://www.joacp.org/article.asp?issn=0970-9185;year=2013;volume=29;issue=1;spage=95;epage=98;aulast=Kansara 
787 0 |n https://doaj.org/toc/0970-9185 
856 4 1 |u https://doaj.org/article/126456e3fe264fc0a99ceec9110f4bdb  |z Connect to this object online.