Abstract
Six cases radiologically and clinically diagnosed Holt-Oram Syndrome are reported. Two of the cases are familial and the others are caused by de novo mutation. One, has preaksial polydactyly which is an uncommon finding in this syndrome.
Copyright and license
Copyright © 1980 The Author(s). This is an open access article distributed under the Creative Commons Attribution License (CC BY), which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is properly cited.
How to cite
1.
Tunçbilek E, Özme Ş, Besim A, Balcı S. Holt-Oram syndrome (analysis of six cases). Turk J Pediatr 1980; 22: 50-58. https://doi.org/10.24953/turkjpediatr.1980.4150