Holt-Oram Syndrome

A maIe child who had a skeletal and cardiovascular anomaly relaled with Synrome and esotropia was presented. On !his palient following symptoms were observed; bilaterally hypoplasique arm, 3 fingers on the right and 4 flngers on the left hand, arrioseptal defect and on the. eye 35 prisin diopri esoıropia, in the pedigri, tl was stated that was a first mutation occurred in mother.