Özet:

Pallister-Killian syndrome is a rare genetic disorder characterized by craniofacial dysmorphism, growth retardation, mental retardation, hypotonia, seizures, vision and hearing disorders, congenital malformations and congenital heart disease. Ventricular septal defect and atrial septal defect are the most common cardiac malformations. Arthmias have been rarely in these patients. In this case report, recurrent ventricular tachycardia episodes were an eleven years old patient with Pallister-Killian syndrome and wanted to emphasize that patients with Pallister Killian syndrome should be screened for the arrhythmia.

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