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Article

Genetic aspects of Hirschsprung's disease.

Seminars in pediatric surgery - 1 Aug 1998

Kusafuka T, Puri P

Abstract excerpt

Hirschsprung's disease (HD) is a relatively common cause of intestinal obstruction in the newborn, characterized by the absence of autonomic ganglion cells in the terminal bowel. Existence of familial cases indicates that genetic factors may be involved in the etiology of some cases of HD. Different inheritance patterns observed in subsets of HD families or kindreds, and the detection of different chromosome...

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PMID: 9718652
DOI: 10.1016/s1055-8586(98)70010-1

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RET

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

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