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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Detalles Bibliográficos
Autores principales: Kansara, Bhuvnesh, Singh, Ajmer, Girotra, Samir, Iyer, K S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590552/
https://www.ncbi.nlm.nih.gov/pubmed/23493844
http://dx.doi.org/10.4103/0970-9185.105812

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590552/
https://www.ncbi.nlm.nih.gov/pubmed/23493844
http://dx.doi.org/10.4103/0970-9185.105812

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