Kevin Moses Hanky Jr Tandayu, Yovi Kurniawati, Indriwanto Sakidjan Atmosudigdo, Oktavia Lilyasari
National Cardiovascular Centre Harapan Kita and Universitas Indonesia.
Indonesia
Annals of Pediatric Cardiology
Ann Pediatr Cardiol 2023; 16: 374-377
DOI: 10.4103/apc.apc_109_23
Abstract
Berry syndrome is an extremely rare constellation of several congenital cardiac anomalies consisting of aortopulmonary window, aortic origin of the right pulmonary artery (AORPA), interrupted aortic arch or hypoplastic aortic arch or coarctation of the aorta, and an intact ventricular septum with high neonatal mortality rates. The disease is fatal with high mortality (90%) in the neonatal period with surviving patients mostly developing pulmonary hypertension. We describe the clinical presentation and diagnostic clues in two patients with Berry syndrome.
Category
Class I. Pulmonary Hypertension Associated with Congenital Cardiovascular Disease
Abnormal Systemic to Pulmonary Arterial Collaterals or Connections
Age Focus: Pediatric Pulmonary Vascular Disease
Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication
Article Access
Free PDF File or Full Text Article Available Through PubMed or DOI: Yes