Discordance for Cornelia de Lange syndrome in twins.
- 1 October 1976
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 13 (5) , 402-404
- https://doi.org/10.1136/jmg.13.5.402
Abstract
A male infant, the 1st-born of twins, with features of Cornelia de Lange syndrome is described. His normal twin was discordant for 3 of the 14 blood loci tested. Chromosomes from the affected infant appeared normal. Although the etiological basis for the Cornelia de Lange syndrome remains obscure, most authorities accept genetic rather than environmental causation. The present findings of discordance for Cornelia de Lange syndrome in twins support this view but do not clarify the mode of inheritance.This publication has 4 references indexed in Scilit:
- Studies of Malformation Syndromes XXVAHuman Heredity, 1971
- DE LANGE SYNDROME - REPORT OF 20 CASES1967
- [Cornelia de Lange syndrome I in twins (Amsterdam type of degeneration)].1966
- BRACHMANN‐DE LANGE SYNDROME: A report of four casesJournal of Paediatrics and Child Health, 1965