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Arch Dis Child 78:316-322 doi:10.1136/adc.78.4.316
  • Original article

Congenital central hypoventilation syndrome and Hirschsprung’s disease

  1. G D H Croakera,
  2. E Shib,
  3. E Simpsonc,
  4. T Cartmilla,
  5. D T Cassa
  1. aRoyal Alexanda Hospital for Children, Sydney, Australia, bSydney Children’s Hospital, Sydney, Australia, cWoden Valley Hospital, Canberra, Australia
  1. Dr G D H Croaker, Department of Surgical Research, Royal Alexandra Hospital for Children, Westmead, NSW 2145, Australia.
  • Accepted 2 December 1997

Abstract

Five cases of the Hirschsprung’s disease–congenital central hypoventilation syndrome (CCHS) association are presented and 41 other published cases reviewed. These children have a distinct pattern of associated features, an equal sex incidence, and a characteristic spectrum of disease severity which suggests that the condition is genetically distinct from other cases of Hirschsprung’s disease. While approximately 1.5% of Hirschsprung’s disease patients, and 10% of those with total colonic aganglionosis, will have CCHS, up to 50% of CCHS patients will have Hirschsprung’s disease. Approximately 20% of CCHS/Hirschsprung patients will also have neuroblastoma or ganglioneuroma, usually multiple. Abnormalities of the eye and autonomic nervous system are also common. The ventilatory abnormality is usually evident on the first day of life. The aganglionosis is also severe, with more than half (59%) of the patients having aganglionosis extending into the small bowel.

Footnotes