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Congenital heart defects in isolated and syndromic context

dc.contributor.authorSilva, Cátia
dc.contributor.authorVarela, Catarina
dc.contributor.authorAlmeida, Cláudia
dc.contributor.authorGomes, Marcos
dc.contributor.authorBrochado, Paulo
dc.contributor.authorNogueira, Rosete
dc.date.accessioned2022-03-09T18:09:35Z
dc.date.available2022-03-09T18:09:35Z
dc.date.issued2015-11
dc.description.abstractCongenital heart defects (CHD) is defined as a coarse structural abnormality of the heart or intrathoracic large vessels and which has functional significance. The objectives of this study were to determine the percentage of CHD in fetal autopsies and its frequency in isolated and syndromic context evaluate the most frequent types of CHD and determine the impact of histological study in the diagnosis of cardiac structural abnormalities.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSilva, C., Varela, C., Almeida, C., Gomes, M., Brochado, P., & Nogueira, R. (2015). Congenital heart defects in isolated and syndromic context. In R. A. Silva, P. Baylina, F. Q. Vieira, C. Barrias, M. Rubim, T. Coelho, C. Prudêncio, & Â. Jesus (Eds.), II Congresso Internacional da Saúde Gaia Porto: Livro de Resumos (1st ed., Vol. 1, pp. 137). Escola Superior de Tecnologia da Saúde do Instituto Politécnico do Porto.pt_PT
dc.identifier.isbn978-989-20-6340-9
dc.identifier.urihttp://hdl.handle.net/10400.22/20186
dc.language.isoengpt_PT
dc.publisherEscola Superior de Tecnologia da Saúde do Instituto Politécnico do Portopt_PT
dc.relation.ispartofseriesP;43
dc.titleCongenital heart defects in isolated and syndromic contextpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlacePortopt_PT
oaire.citation.issue1pt_PT
oaire.citation.startPage137pt_PT
oaire.citation.titleII Congresso Internacional da Saúde Gaia Porto: Livro de Resumospt_PT
oaire.citation.volume1pt_PT
person.familyNameSilva
person.givenNameCátia
person.identifier.ciencia-id5318-DCFD-218D
person.identifier.orcid0000-0001-8306-4568
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublication5eebf2bb-32f6-4593-a536-6db611d531e8
relation.isAuthorOfPublication.latestForDiscovery5eebf2bb-32f6-4593-a536-6db611d531e8

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