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Article

The contribution of associated congenital anomalies in understanding Hirschsprung's disease.

Pediatric surgery international - 1 Apr 2006

Moore S W

Abstract excerpt

Hirschsprung's disease (HSCR) is a complex congenital disorder which, from a molecular perspective, appears to result due to disruption of normal signalling during development of enteric nerve cells, resulting in aganglionosis of the distal bowel. Associated congenital anomalies occur in at least...

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Identifiers

PMID: 16518596
DOI: 10.1007/s00383-006-1655-2

Genes

RET
EDNRB

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16518596-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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