Literature DB >> 2688422

Familial duodenal atresia: a report of two families and review.

L G Best1, N E Wiseman, A E Chudley.   

Abstract

We report on 2 families with recurrence of uncomplicated duodenal atresia. The presence of consanguinity in one family, the frequent occurrence of consanguinity in parents of affected children previously reported, and the equal sex ratio suggest autosomal recessive inheritance.

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Year:  1989        PMID： 2688422     DOI： 10.1002/ajmg.1320340322

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


  3 in total

1.  Double bubble, double trouble.

Authors:  H Okti Poki; A J A Holland; J Pitkin
Journal:  Pediatr Surg Int       Date:  2005-05-24       Impact factor: 1.827

2.  Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia.

Authors:  H G Brunner; R M Winter
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

Review 3.  The Role of Fibroblast Growth Factor 10 Signaling in Duodenal Atresia.

Authors:  Matthew L M Jones; Gulcan Sarila; Pierre Chapuis; John M Hutson; Sebastian K King; Warwick J Teague
Journal:  Front Pharmacol       Date:  2020-03-10       Impact factor: 5.810
  3 in total

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