Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome.
Open Access
- 1 February 1985
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 22 (1) , 36-38
- https://doi.org/10.1136/jmg.22.1.36
Abstract
A newly recognised profound limb deficiency malformation syndrome in two Arab sibs of different sexes with consanguineous parents is described. Additional features, which include thoracic dystrophy, unusual facies, and normal intelligence, are consistent in both of them. Autosomal recessive inheritance is suggested.This publication has 1 reference indexed in Scilit: