Prenatally closed gastroschisis with midgut atresia

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dc.contributor.authorBasaran, UN
dc.contributor.authorInan, M
dc.contributor.authorGücer, F
dc.contributor.authorYardim, T
dc.contributor.authorPul, M
dc.date.accessioned2024-06-12T11:02:31Z
dc.date.available2024-06-12T11:02:31Z
dc.date.issued2002
dc.departmentTrakya Üniversitesien_US
dc.description.abstractSpontaneous prenatal closure of gastroschisis (GS) is rare and usually associated with atresia of the midgut. We describe a case of GS diagnosed at 20 weeks' gestation that resolved spontaneously in utero. At delivery the infant had an ileus. A laparotomy with a jejunocolostomy was performed, but she died at 2 months of age due to complications of total parenteral nutrition.en_US
dc.identifier.doi10.1007/s00383-002-0815-2
dc.identifier.endpage552en_US
dc.identifier.issn0179-0358
dc.identifier.issue5-6en_US
dc.identifier.pmid12415410en_US
dc.identifier.scopus2-s2.0-0036730756en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage550en_US
dc.identifier.urihttps://doi.org/10.1007/s00383-002-0815-2
dc.identifier.urihttps://hdl.handle.net/20.500.14551/21306
dc.identifier.volume18en_US
dc.identifier.wosWOS:000179508000070en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherSpringer-Verlagen_US
dc.relation.ispartofPediatric Surgery Internationalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGastroschisisen_US
dc.subjectFetal Abdominal-Wall Closureen_US
dc.subjectIntestinal Atresiaen_US
dc.subjectShort-Bowel Syndromeen_US
dc.subjectVanishing Bowelen_US
dc.subjectManagementen_US
dc.subjectClosureen_US
dc.subjectDefecten_US
dc.titlePrenatally closed gastroschisis with midgut atresiaen_US
dc.typeArticleen_US

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