Literature DB >> 155396

Familial occurrence of gastroschisis. Four new cases and review of the literature.

C F Salinas, L Bartoshesky, H B Othersen, L Leape, M Feingold, R J Jorgenson.   

Abstract

In two unrelated families, there was familial occurrence of gastroschisis. In one family, a boy and girl were affected and there was a family history of stillbirth, abortion, prematurity, and esophageal obstruction. In the second family, two boys were affected and there was a family history of spontaneous abortion, inguinal hernia, and umbilical hernia. The recurrence of gastroschisis, generally considered a sporadic congenital effect, suggests that the condition may be genetic in nature. Furthermore, the pedigree of one of the families suggests that gastroschisis may be a severe expression of umbilical hernia or other abdominal wall defects. Autosomal dominant inheritance with variable expressivity or multifactorial inheritance may explain the occurrence of gastroschisis in the two families. Thus, a family history of abdominal wall defects may increase the risk for gastroschisis.

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Year:  1979        PMID: 155396

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  2 in total

1.  Gastroschisis and omphalocele in Finland in the 1970s: prevalence at birth and its correlates.

Authors:  K Hemminki; I Saloniemi; P Kyyrönen; M Kekomäki
Journal:  J Epidemiol Community Health       Date:  1982-12       Impact factor: 3.710

2.  Familial gastroschisis and omphalocele.

Authors:  R B Lowry; P A Baird
Journal:  Am J Hum Genet       Date:  1982-05       Impact factor: 11.025

  2 in total

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