Congenital anal anomalies in two families with the Opitz G syndrome.
- 1 November 1987
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 24 (11) , 688-691
- https://doi.org/10.1136/jmg.24.11.688
Abstract
Five children from two families presented to a regional neonatal surgical unit between 1959 and 1984 with congenital anal anomalies and other malformations resulting from an autosomal dominant inherited condition, the Opitz G syndrome. This and other Mendelian causes of congenital anal malformations are briefly discussed in view of their importance for genetic counseling.This publication has 4 references indexed in Scilit:
- Prenatal treatment of fetal hydrops associated with the hypertelorism‐dysphagia syndrome (opitz‐g syndrome)Prenatal Diagnosis, 1986
- Male to male transmission of the G syndromeClinical Genetics, 1983
- Congenital malformations in singletons: epidemiologic survey. Report from the Collaborative Perinatal project.1974
- The G SyndromeArchives of Pediatrics & Adolescent Medicine, 1971