Literature DB >> 12415410

Prenatally closed gastroschisis with midgut atresia.

Umit Nusret Basaran1, Mustafa Inan, Fatih Gücer, Turgut Yardim, Mehmet Pul.   

Abstract

Spontaneous 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.

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Year:  2002        PMID: 12415410     DOI: 10.1007/s00383-002-0815-2

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  5 in total

Review 1.  Successful management of short gut due to vanishing gastroschisis - case report and review of the literature.

Authors:  B A Khalil; J C Gillham; L Foresythe; R Harding; T Johnston; C Wright; A Morabito
Journal:  Ann R Coll Surg Engl       Date:  2010-06-07       Impact factor: 1.891

2.  Total absence of the small bowel in a premature neonate.

Authors:  Gail E Besner; Gregory D Bates; Carl P Boesel; Vivekanand Singh; Stephen E Welty; Cynthia A Corpron
Journal:  Pediatr Surg Int       Date:  2005-04-05       Impact factor: 1.827

3.  Gastroschisis with jejunal and colonic atresia, and isolated colonic atresia in dichorionic, diamniotic twins.

Authors:  Matthew A Saxonhouse; David W Kays; David J Burchfield; Roger Hoover; Saleem Islam
Journal:  Pediatr Surg Int       Date:  2009-03-24       Impact factor: 1.827

4.  Closed Gastroschisis.

Authors:  Mohammed Abdel-Latif; Mohamed H Soliman; Khaled M El-Asmar; Mohamed Abdel-Sattar; Ibrahim M Abdelraheem; Ehab El-Shafei
Journal:  J Neonatal Surg       Date:  2017-08-10

5.  Vanishing Gastroschisis with a Favorable Outcome after a 3-Year Follow-Up: A Case Report and Literature Review.

Authors:  Elise Abi Rached; N Sananes; I Kauffmann-Chevalier; F Becmeur
Journal:  Case Rep Obstet Gynecol       Date:  2020-01-07
  5 in total

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