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Congenital medium sternal cleft with partial ectopia cordis repair

dc.contributor.authorSousa, P. R.
dc.contributor.authorAntunes, S.
dc.contributor.authorCouto, A.
dc.contributor.authorSantos, G. C.
dc.contributor.authorLeal, L. G.
dc.contributor.authorMagalhaes, M. P.
dc.contributor.authorMadeira Island, Região Autónoma da Madeira
dc.contributor.authorPortugal
dc.date.accessioned2021-01-12T17:38:59Z
dc.date.available2021-01-12T17:38:59Z
dc.date.issued2009-09-15
dc.description.abstractCongenital sternal malformation is a rare anomaly often diagnosed as an asymptomatic condition at birth. The authors report a clinical case of a full-term female neonate with congenital sternal cleft and partial ectopia cordis. Successful surgical repair was accomplished at 6 days of age. When surgery is performed shortly after birth, the procedure is easier and better results are achieved.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSousa PR, Antunes S, Couto A, et al. Congenital medium sternal cleft with partial ectopia cordis repair. Case Reports 2009;2009:bcr0620092018.pt_PT
dc.identifier.doi10.1136/bcr.06.2009.2018pt_PT
dc.identifier.issn1757-790x
dc.identifier.urihttp://hdl.handle.net/10400.26/34680
dc.language.isoengpt_PT
dc.publisherBMJ Publishing Group Ldapt_PT
dc.subjectcongenital medium sternal cleftpt_PT
dc.subjectpartial ectopia cordis repairpt_PT
dc.subjectsurgical repairpt_PT
dc.subjectneonatologypt_PT
dc.subjectMadeira Islandpt_PT
dc.subjectRegião Autónoma da Madeirapt_PT
dc.subjectPortugalpt_PT
dc.titleCongenital medium sternal cleft with partial ectopia cordis repairpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPagebcr0620092018pt_PT
oaire.citation.issuesep15 2pt_PT
oaire.citation.startPagebcr0620092018pt_PT
oaire.citation.titleCase Reportspt_PT
oaire.citation.volume2009pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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