Berry syndrome—a rare congenital cardiac anomaly
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine,Surgery
Link
https://link.springer.com/content/pdf/10.1007/s12055-021-01206-0.pdf
Reference32 articles.
1. Berry TE, Bharati S, Muster AJ, et al. Distal aortopulmonary septal defect, aortic origin of the right pulmonary artery, intact ventricular septum, patent ductus arteriosus and hypoplasia of the aortic isthmus: a newly recognized syndrome. Am J Cardiol. 1982;49:108–16.
2. Hu R, Zhang W, Liu X, Dong W, Zhu H, Zhang H. Current outcomes of one-stage surgical correction for Berry syndrome. J Thorac Cardiovasc Surg. 2017;153:1139–47.
3. Murin P, Sinzobahamvya N, Ch Blaschczok H, et al. Aortopulmonary window associated with interrupted aortic arch: report of surgical repair of eight cases and review of literature. Thorac Cardiovasc Surg.2012; 60:215–220.
4. Kutsche LM, Van Mierop LH. Anatomy and pathogenesis of aorticopulmonary septal defect. Am J Cardiol. 1987;59:443–7.
5. Jayaram N, Knowlton J, Shah S, Gelatt M, Lofland G, Raghuveer G. Berry syndrome: a possible genetic link. Pediatr Cardiol. 2013;34:1511–3.
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1. Berry syndrome: a rare cause of cardiac failure in the early neonatal period;BMJ Case Reports;2022-11
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