Hirschsprung's disease and congenital deafness
- 1 January 1977
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 38 (2) , 157-161
- https://doi.org/10.1007/bf00527397
Abstract
A family is described showing deafness in three consecutive generations. Hirschsprung's disease was present in at least two of the affected patients and a history of bowel dysfunction was present in the third. The association of the two disorders in this family may be due to a single autosomal dominant gene and in this regard differs from previously reported isolated patients with Hirschsprung's disease and deafness.This publication has 4 references indexed in Scilit:
- Letter: Hirschsprung's disease and congenital deafness.Journal of Medical Genetics, 1975
- Hirschsprung's Disease and Congenital DeafnessJournal of Medical Genetics, 1973
- The Genetics of Hirschsprung's DiseaseNew England Journal of Medicine, 1967
- A family study of Hirschsprung's diseaseAnnals of Human Genetics, 1963