Abstract
There is a rare combination of cardiac anomalies, consists of aortopulmonary window (APW); aortic origin of the right pulmonary artery; interrupted aortic arch (IAA) or hypoplastic aortic arch or coarctation of the aorta; and an intact ventricular septum called Berry Syndrome. While much less is known in Russian literature about the clinical features, diagnosis, treatment, and outcomes of Berry syndrome, World’s literature very limited data there are as well. This publication reviews some cases published since 1982 on Berry syndrome. The aim of this article is to discuss the various surgical techniques and approaches available for this extremely rare group of patients, scrutinizing on the surgical decisions that makes the personal patient’s management. Any Berry syndrome. As it turns out, patients with Berry syndrome are a rare but wellidentified and surgically correctable anomaly.
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About the authors
- Aleksey E. Chernogrivov, Dr. Med. Sci., Cardiovascular Surgeon, Chief Researcher; ORCID
- Inessa E. Nefedova, Dr. Med. Sci., Pediatric Cardiologist, Head of Department of cardiovascular surgery 1 (Emergency Surgery in premature newborns and infants (up to 1 y.o.) with congenital heart defects; ORCID
- Elizaveta S. Dorokhina, Cardiovascular Surgeon; ORCID
- Anatoliy E. Tagaev, Cardiovascular Surgeon; ORCID
- Maksim V. Makhalin, Senior Researcher, Cardiovascular Surgeon; ORCID