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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: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3590552/ https://ncbi.nlm.nih.gov/pubmed/23493844 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0970-9185.105812 |
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