Article
[Genetics of Hirschsprung disease].
Comptes rendus des seances de la Societe de biologie et de ses filiales - 1 Jan 1996
Attié T, Salomon R, Amiel J, Edery P, Pelet A, Nihoul-Fékété C, Munnich A, Lyonnet S
Abstract excerpt
Hirschsprung disease (HD) is one of the commonest gastro-intestinal malformations, as it affects one child out of 5,000 births. It classically induces severe neonatal intestinal obstruction requiring surgical treatment which currently ensures a favourable prognosis for most of the affected childr...
Topics
- Endothelin-3
- Female
- Hirschsprung Disease
- Humans
- Male
- Mutation
- Proto-Oncogene Mas
- Proto-Oncogenes
- Receptors, Endothelin
