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.

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