Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease

Eur J Hum Genet. 1997 Jul-Aug;5(4):247-51.


Hirschsprung disease (HSCR, aganglionic megacolon) is a frequent congenital malformation regarded as a multigenic neurocristopathy. Four susceptibility genes have recently been identified in HSCR, namely the RET proto-oncogene, the glial cell line-derived neurotrophic factor (GDNF), the endothelin B receptor (EDNRB) and the endothelin-3 genes (EDN3). Homozygosity for EDN3 mutations has been previously shown to cause the Shah-Waardenburg syndrome, a combination of HSCR with features of the Waardenburg syndrome. Here, we report on heterozygous EDN3 missense mutations in isolatec HSCR. The present data give further support to the role of the endothelin signaling pathway in the development of neural crest-derived enteric neurons. They also suggest the possibility that either recessive or weakly penetrant dominant alleles could occur at the EDN3 locus, depending on the nature of the mutation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endothelin-3 / genetics*
  • Exons
  • Female
  • Heterozygote
  • Hirschsprung Disease / genetics*
  • Humans
  • Male
  • Mutation*
  • Pedigree
  • Polymorphism, Single-Stranded Conformational
  • Proto-Oncogene Mas
  • Syndrome
  • Waardenburg Syndrome / genetics


  • Endothelin-3
  • MAS1 protein, human
  • Proto-Oncogene Mas