Literature DB >> 31993350

Gastrointestinal diseases among relatives of patients with esophageal atresia with or without tracheoesophageal fistula.

Florian Zeck1, Heiko Reutter1,2.   

Abstract

BACKGROUND: Several studies have identified genetic factors that are associated with the formation of isolated and non-isolated esophageal atresia with or without tracheoesophageal fistula (EA/TEF) in human and mice. Some of these genetic factors like FOXF1/Foxf1 are associated with Barrett syndrome, esophageal carcinoma or tumors of the gastrointestinal tract. Here, we investigated the prevalence of common gastrointestinal diseases among EA/TEF patients and their first- and second-degree relatives (parents and grandparents).
METHODS: We send out a questionnaire to 280 EA/TEF families asking for the presence of Barrett syndrome, Achalasia and carcinoma of the esophagus, the stomach, the small and large intestine among first- and second-degree relatives.
RESULTS: In 32 of 124 families we found at least one affected family member with a possible association of colon carcinoma and the occurrence of EA/TEF within the same family.
CONCLUSIONS: Further studies are needed to evaluate a possible association. 2019 Translational Pediatrics. All rights reserved.

Entities:  

Keywords:  Esophageal atresia (EA); gastrointestinal disease; genetic risk factors

Year:  2019        PMID: 31993350      PMCID: PMC6970114          DOI: 10.21037/tp.2019.04.01

Source DB:  PubMed          Journal:  Transl Pediatr        ISSN: 2224-4336


  13 in total

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8.  Achalasia in Iceland, 1952-2002: an epidemiologic study.

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Journal:  Dig Dis Sci       Date:  2007-04-10       Impact factor: 3.199

9.  Haploinsufficiency of the forkhead gene Foxf1, a target for sonic hedgehog signaling, causes lung and foregut malformations.

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Authors:  Jayabal Panneerselvam; Anna Pickering; Jun Zhang; Hong Wang; Hui Tian; Junnian Zheng; Peiwen Fei
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