Genetic alterations in necrotizing enterocolitis

Abstract An underlying genetic predisposition to necrotizing enterocolitis (NEC) is increasingly being recognized. Candidate gene or pathway approaches as well as genome-wide approaches are beginning to identify potential pathogenic variants for NEC in premature infants. However, a majority of these...

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Published inSeminars in perinatology Vol. 41; no. 1; pp. 61 - 69
Main Authors Cuna, Alain, MD, Sampath, Venkatesh, MD
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.02.2017
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Summary:Abstract An underlying genetic predisposition to necrotizing enterocolitis (NEC) is increasingly being recognized. Candidate gene or pathway approaches as well as genome-wide approaches are beginning to identify potential pathogenic variants for NEC in premature infants. However, a majority of these studies have not yielded definitive results because of limited sample size and lack of validation. Despite these challenges, understanding the contribution of genetic variation to NEC is important for providing new insights into the pathogenesis of NEC as well as allowing for targeted care of infants with inherent susceptibility. In this review we provide a summary of published genetic association studies in NEC along with defining the challenges and possible future approaches.
Bibliography:ObjectType-Article-2
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ObjectType-Review-1
ISSN:0146-0005
1558-075X
DOI:10.1053/j.semperi.2016.09.019