Large aortic aneurysm and dissection in a patient with Marfan’s syndrome
dc.contributor.author | Pivatto Junior, Fernando | pt_BR |
dc.contributor.author | Ramos, Leila Denise Cardoso | pt_BR |
dc.contributor.author | Foppa, Murilo | pt_BR |
dc.contributor.author | Torres, Felipe Soares | pt_BR |
dc.date.accessioned | 2017-05-30T02:37:08Z | pt_BR |
dc.date.issued | 2015 | pt_BR |
dc.identifier.issn | 2357-9730 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/10183/158725 | pt_BR |
dc.description.abstract | Marfan’s syndrome is an autosomal dominant disorder of connective tissue affecting approximately 1 in 5000 people. In individuals with this syndrome, more than 90% of deaths from known causes result from cardiovascular complications, such as aortic dissection, aortic regurgitation, and congestive cardiac failure. In this report, we present a patient with a large symptomatic aortic aneurysm and chronic dissection, severe aortic regurgitation and cardiomegaly, treated successfully with resection of the proximal aorta and placement of a mechanic aortic valved graft. | en |
dc.format.mimetype | application/pdf | |
dc.language.iso | eng | pt_BR |
dc.relation.ispartof | Clinical and biomedical research. Porto Alegre. Vol. 35, n. 2, (2015), p. 112-115 | pt_BR |
dc.rights | Open Access | en |
dc.subject | Síndrome de Marfan | pt_BR |
dc.subject | Marfan’s syndrome | en |
dc.subject | Aortic aneurysm | en |
dc.subject | Aneurisma aórtico | pt_BR |
dc.subject | Dissecação | pt_BR |
dc.subject | Dissection | en |
dc.title | Large aortic aneurysm and dissection in a patient with Marfan’s syndrome | pt_BR |
dc.type | Artigo de periódico | pt_BR |
dc.identifier.nrb | 001013006 | pt_BR |
dc.type.origin | Nacional | pt_BR |
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