Hirschsprung's disease, Ondine's curse, and neuroblastoma--manifestations of neurocristopathy
- PMID: 3222062
- DOI: 10.1007/BF02388410
Hirschsprung's disease, Ondine's curse, and neuroblastoma--manifestations of neurocristopathy
Abstract
The term neurocristopathy has been applied to the association of Hirschsprung's disease, Ondine's curse (Congenital Hypoventilation Syndrome) and congenital neuroblastoma. Eight newborns with Hirschsprung's disease and Ondine's curse are discussed. Five of these have been seen by the authors. The remaining three patients are reported in the literature. In six of the infants (5 of ours, 1 from the literature) total colonic aganglionosis was found. Congenital neuroblastoma was present in two of the infants. In infants presenting with Hirschsprung's disease (especially of the long segment type) and breathing difficulties, the presence of a neurocristopathy should be considered.
Comment in
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Hirschsprungs disease, Ondine's curse, and neuroblastoma--manifestations of neurocristopathy.Pediatr Radiol. 1989;20(1-2):136. doi: 10.1007/BF02010663. Pediatr Radiol. 1989. PMID: 2602008 No abstract available.
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