Literature DB >> 34511759

Berry syndrome-a rare congenital cardiac anomaly.

Maruti Haranal1, Balaji Srimurugan2, Duyen Mai Dinh1, Sivakumar Sivalingam1.   

Abstract

Berry syndrome is a rare congenital cardiac anomaly, characterized by distal aortopulmonary window, hypoplasia or interruption of the aortic arch, intact ventricular septum, and aortic origin of the right pulmonary artery and patent ductus arteriosus. Anatomic depiction of each component is important for the diagnosis. Single-stage surgical repair is challenging but feasible with good survival outcomes. The available literature on this anomaly is limited. Hence, this paper aims at reviewing the literature on Berry syndrome. © Indian Association of Cardiovascular-Thoracic Surgeons 2021.

Entities:  

Keywords:  Aortopulmonary window; Berry syndrome; Interrupted aortic arch; Right pulmonary artery

Year:  2021        PMID: 34511759      PMCID: PMC8387542          DOI: 10.1007/s12055-021-01206-0

Source DB:  PubMed          Journal:  Indian J Thorac Cardiovasc Surg        ISSN: 0970-9134


  31 in total

1.  Berry syndrome with trisomy 13.

Authors:  J Sharma; M Saleh; B B Das
Journal:  Pediatr Cardiol       Date:  2002-02-19       Impact factor: 1.655

2.  Anomalous origin of the left coronary artery from the main pulmonary artery associated with Berry syndrome.

Authors:  Hideaki Senzaki; Haruhiko Asano; Satoshi Masutani; Tamotu Matunaga; Hirotaka Ishido; Mio Taketatu; Toshiki Kobayashi; Nozomu Sasaki; Shunei Kyo; Yuji Yokote
Journal:  J Thorac Cardiovasc Surg       Date:  2003-11       Impact factor: 5.209

3.  Berry syndrome: two cases of successful surgical repair.

Authors:  Seong Yong Park; Hyun-Chul Joo; Young-Nam Youn; Young-Hwan Park; Han Ki Park
Journal:  Circ J       Date:  2008-03       Impact factor: 2.993

4.  One-stage repair of absence of the aortopulmonary septum and interrupted aortic arch.

Authors:  W X Ding; Z K Su; D F Cao; R A Jonas
Journal:  Ann Thorac Surg       Date:  1990-04       Impact factor: 4.330

5.  Berry syndrome, a complex aortopulmonary malformation: one-stage repair in a neonate.

Authors:  P A Abbruzzese; M Merlo; E Chiappa; R Bianco; F Ferrero; C M Cappone
Journal:  Ann Thorac Surg       Date:  1997-10       Impact factor: 4.330

6.  Berry syndrome: the importance of genetic evaluation before surgical intervention.

Authors:  Juan I Remon; David A Briston; Kenan W Stern
Journal:  Cardiol Young       Date:  2015-04-01       Impact factor: 1.093

7.  Surgical management of aortopulmonary window associated with interrupted aortic arch: a Congenital Heart Surgeons Society study.

Authors:  Igor E Konstantinov; Tara Karamlou; William G Williams; Jan M Quaegebeur; Pedro J del Nido; Thomas L Spray; Christopher A Caldarone; Eugene H Blackstone; Brian W McCrindle
Journal:  J Thorac Cardiovasc Surg       Date:  2006-05       Impact factor: 5.209

8.  Diagnosis of Berry syndrome in an infant by two-dimensional and color Doppler echocardiography.

Authors:  C Alva-Espinosa; S Jiménez-Arteaga; E Díaz-Díaz; A Martínez-Sanchez; D Jiménez-Zepeda; J Mojarro-Ríos; C Meléndez-López
Journal:  Pediatr Cardiol       Date:  1995 Jan-Feb       Impact factor: 1.655

9.  Current Outcomes of Surgical Management of Aortopulmonary Window and Associated Cardiac Lesions.

Authors:  Bahaaldin Alsoufi; Brian Schlosser; Courtney McCracken; Brian Kogon; Kirk Kanter; William Border; Ritu Sachdeva
Journal:  Ann Thorac Surg       Date:  2016-05-18       Impact factor: 4.330

10.  Surgical management of aortopulmonary window: a 40-year experience.

Authors:  C L Backer; C Mavroudis
Journal:  Eur J Cardiothorac Surg       Date:  2002-05       Impact factor: 4.191

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.