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Prenatally detected gastroschisis presenting as jejunal atresia due to vanishing bowel

dc.contributor.authorSarimurat, N
dc.contributor.authorCelayir, S
dc.contributor.authorYeker, D
dc.contributor.authorBesik, C
dc.date.accessioned2021-03-02T20:05:46Z
dc.date.available2021-03-02T20:05:46Z
dc.date.issued1999
dc.identifier.citationCelayir S., Besik C., Sarimurat N., Yeker D., "Prenatally detected gastroschisis presenting as jejunal atresia due to vanishing bowel", PEDIATRIC SURGERY INTERNATIONAL, cilt.15, sa.8, ss.582-583, 1999
dc.identifier.issn0179-0358
dc.identifier.otherav_003e2144-dca9-4d77-89a5-13588d1fe3af
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/6149
dc.identifier.urihttps://doi.org/10.1007/s003830050678
dc.description.abstractA case of gastroschisis complicated by vanishing bowel and presenting as jejunal atresia is reported that is uniquely different from previously reported cases. Following delivery, complete closure of the abdominal wall with a small fascial defect was observed. Complete healing of this fascial defect was observed at 1 month of age.
dc.language.isoeng
dc.subjectCerrahi Tıp Bilimleri
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectCERRAHİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titlePrenatally detected gastroschisis presenting as jejunal atresia due to vanishing bowel
dc.typeMakale
dc.relation.journalPEDIATRIC SURGERY INTERNATIONAL
dc.contributor.department, ,
dc.identifier.volume15
dc.identifier.issue8
dc.identifier.startpage582
dc.identifier.endpage583
dc.contributor.firstauthorID124186


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