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Association analysis of NOX5 polymorphisms with Hirschsprung disease

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Topic overview

Replication study of 187 HSCR patients identifies six NOX5 gene variants significantly associated with Hirschsprung disease risk, with strongest association at rs62010828. Subgroup analysis reveals distinct genetic patterns for long-segment HSCR and TCA subtypes, supporting NOX5 as a candidate susceptibility gene.

Keywords

Hirschsprung Disease Nox5 Polymorphisms Genome-wide Association Study Pediatric Gastroenterology Genetic Susceptibility Enteric Nervous System Long-segment Hscr

Hashtags

#HirschsprungDisease #PediatricGenetics #GWAS #EntericNervousSystem

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How to cite: GlobalCastMD. Association analysis of NOX5 polymorphisms with Hirschsprung disease. GlobalCastMD Medical Library. 2019-01-24. https://library.globalcastmd.com/article/1127

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