All issues > Volume 41(4); 1998

Case Report

J Korean Pediatr Soc. 1998;41(4):543-547. Published online April 15, 1998.

A Case of Berry Syndrome associated with Syndactyly

Sang Chun SC Jung¹, Kyoung Sim KS Kim¹, Yong Wook YW Kim¹, Ki Bok KB Kim¹

¹Department of Pediatrics, Kwangju Christian Hospital, Kwangju, Korea

Correspondence Sang Chun SC Jung ,Email: 1

Abstract

Berry syndrome is a rare association of congenital heart anomalies which consists of a distal aortopulmonary window with aortic origin of the right pulmonary artery and hypoplasia or interruption of the aortic arch. This defect can be corrected only by immediate surgical intervention, so accurate preoperative diagnosis and detailed anatomic depiction of this syndrome are important in prognosis. We experienced a case of Berry syndrome in an 8-day-old male, who had presented with multiple malformation such as syndactyly, high arched palate and brain hemorrhage. The diagnosis was made by two-dimensional echocardiography. The case is presented with a brief review of related literatures.

Keywords :Berry syndrome, Syndactyly, Two-dimensional echocardiography