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dc.contributor.authorKatranci A.O.
dc.contributor.authorGörk A.S.
dc.contributor.authorRizalar R.
dc.contributor.authorGünaydin M.
dc.contributor.authorAritürk E.
dc.contributor.authorBemay F.
dc.contributor.authorGürses N.
dc.date.accessioned2020-06-21T09:19:17Z
dc.date.available2020-06-21T09:19:17Z
dc.date.issued1998
dc.identifier.issn0019-5456
dc.identifier.urihttps://doi.org/10.1007/BF02849710
dc.identifier.urihttps://hdl.handle.net/20.500.12712/2947
dc.descriptionPubMed: 10771959en_US
dc.description.abstractOmphalocele is often associated with various abnormalities. In two patients admitted with omphalocele, we additionally found defects both in the pars stenalis of diaphragm and in the diaphragmatic surface of the pericardium, sternal defect and tetralogy of Fallot. These entities form the components of a syndrome, named pentalogy of Cantrell. It is extremely in the spectrum of midline closure defects that display wide variations and its incidence is very low. Existing cardiac defect is the most important factor influencing morbidity and mortality. Herein we report two cases of pentalogy of Cantrell with the review of the syndrome in the light of literature.en_US
dc.language.isoengen_US
dc.publisherThe Indian Journal of Pediatricsen_US
dc.relation.isversionof10.1007/BF02849710en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDiaphragmen_US
dc.subjectOmphaloceleen_US
dc.subjectTetralogy of Falloten_US
dc.titlePentalogy of Cantrellen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume65en_US
dc.identifier.issue1en_US
dc.identifier.startpage149en_US
dc.identifier.endpage153en_US
dc.relation.journalIndian Journal of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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