Bilateral renal agenesis, a severe anomaly in a premature infant with VACTERL association: A case report

Basit Öğe Kaydı
dc.contributor.authorBasuguy, Erol
dc.contributor.authorErtuğrul, Sabahattin
dc.contributor.authorAkdeniz, Sevinc
dc.date.accessioned2024-04-24T19:11:14Z
dc.date.available2024-04-24T19:11:14Z
dc.date.issued2017
dc.departmentDicle Üniversitesien_US
dc.description.abstractWe report on a preterm male (birth weight 1,100 g) with bilateral renal agenesis, a lethal malformation. Additionally, the child suffered from an atrial septal defect, ventricular septal defect, right aortic arch anomaly, a high type of anal atresia, vertebral anomalies, limbs defects (VACTERL association). The infant during first day of life was treated with an emergency sigmoid ostomy and peritoneal dialysisbecause of increasing abdominal dilatation and high urea and creatinine levels in blood. Important congenital anomalies associated with VACTERL association and prematurity are very serious causes of mortality in the early perioden_US
dc.identifier.endpage390en_US
dc.identifier.issn2148-2969
dc.identifier.issue6en_US
dc.identifier.startpage387en_US
dc.identifier.trdizinid270023
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/270023
dc.identifier.urihttps://hdl.handle.net/11468/27800
dc.identifier.volume4en_US
dc.indekslendigikaynakTR-Dizin
dc.language.isoenen_US
dc.relation.ispartofPediatric Urology Case Reports
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleBilateral renal agenesis, a severe anomaly in a premature infant with VACTERL association: A case reporten_US
dc.titleBilateral renal agenesis, a severe anomaly in a premature infant with VACTERL association: A case report
dc.typeArticleen_US

Dosyalar

Koleksiyon

TR-Dizin İndeksli Yayınlar Koleksiyonu