Journal article
Hirschsprung disease, postaxial polydactyly, and atrial septal defect
Abstract
We report on an infant girl with Hirschsprung disease, postaxial polydactyly, and atrial septal defect who was born to a consanguineous Iraqi couple. A similar condition of aganglionic megacolon, postaxial polydactyly, and ventricular septal defect with a presumed autosomal recessive (AR) inheritance was reported by Laurence in two sibs [Laurence et al.; J Med Genet 12: 334-338, 1975].
Authors
Nowaczyk MJM; James AG; Superina R; Siegel‐Bartelt J
Journal
American Journal of Medical Genetics, Vol. 68, No. 1, pp. 74–75
Publisher
Wiley
Publication Date
January 10, 1997
DOI
10.1002/(sici)1096-8628(19970110)68:1<74::aid-ajmg14>3.0.co;2-l
ISSN
0148-7299