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A patient with Marfan's syndrome presented with severe rheumatic mitral stenosis and successfully treated with percutaneous transmitral balloon commissurotomy – Report of first case
Marfan's syndrome (MFS) is an inherited autosomal dominant disorder of connective tissue with mutation on the fibrillin-1 gene encoding for fibrillin. This frequently involves the cardiovascular system with prevalence is 1:5000–10,000. The clinical major criteria involve the skeletal and ocular...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3953700/ https://ncbi.nlm.nih.gov/pubmed/24653594 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jcdr.2013.04.002 |
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