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Article

The role of RET genomic variants in infantile hypertrophic pyloric stenosis.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie - 1 Dec 2011

Serra A, Schuchardt K, Genuneit J, Leriche C, Görgens H S, Schackert H-K, Fitze G

Abstract excerpt

Infantile hypertrophic pyloric stenosis (IHPS) is a common childhood pathology affecting approximately 1-5 children pro 1000 newborns, with a genetic background as suggested by the familial occurrence. RET is a candidate gene for IHPS due to its role in the development of the intrinsic innervation and ganglia of the smooth musculature and the association of RET variants with another motility disorder...

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Identifiers

PMID: 22169991
DOI: 10.1055/s-0031-1291357

Genes

RET

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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