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Article

Genetic basis of Hirschsprung's disease.

Pediatric surgery international - 1 Jul 2009

Tam Paul K H, Garcia-Barceló Mercè

Abstract excerpt

Hirschsprung's disease (HSCR) is a developmental disorder characterized by the absence of ganglion cells in the lower digestive tract. Aganglionosis is attributed to a disorder of the enteric nervous system (ENS) whereby ganglion cells fail to innervate the lower gastrointestinal tract during embryonic development. HSCR is a complex disease that results from the interaction of several genes and manifests with...

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Identifiers

PMID: 19521704
DOI: 10.1007/s00383-009-2402-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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