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Ir J Med Sci. 1979 Dec;148(1):100. doi: 10.1007/BF02938060.

A case of Hirschsprung's disease with adrenogenital syndrome and skeletal anomalies.

Irish journal of medical science

A Hayes, R J Fitzgerald

Affiliations

  1. Children's Research Centre, Our Lady's Hospital for Sick Children, Crumlin, Dublin 12.

PMID: 27517398 DOI: 10.1007/BF02938060

Abstract

A girl with adrenogenital syndrome (21-hydroxylase deficiency) and Hirschsprung's disease is described She also had skeletal anomalies. It seems likely that the occurrence of these diseasec in the same patient is coincidental.

References

  1. N Engl J Med. 1967 Jan 19;276(3):138-43 - PubMed
  2. J Pediatr Surg. 1969 Aug;4(4):410-5 - PubMed

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