Abstract
Congenital diaphragmatic hernia is a severe pathology resulting from occurrence defect in diaphragm during fetal development and dislocation abdominal organs to the thoracic cavity that cause lung hypoplasia and pulmonary hypertension. Combination of congenital diaphragmatic hernia and congenital heart defect significantly complicate clinical presentation and surgical correction. In this article we report the case of simultaneous correction of retrosternal diaphragmatic hernia and complete atrioventricular canal in 9-month-old child with Down syndrome.
References
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About the authors
- Konstantin V. Shatalov, Dr. Med. Sc., Professor, Deputy Director, Head of Department, ORCID
- Abdumanap B. Alkhasov, Dr. Med. Sc., Professor, Head of Department,
ORCID
- Magomed A. Abdurazakov, Postgraduate, ORCID
- Irina V. Arnautova, Dr. Med. Sc., Chief Researcher, ORCID
- Rustam R. Akhtyamov, Cardiovascular Surgeon
- Konstantine M. Dzhidzhikhiya, Cand. Med. Sc., Cardiovascular Surgeon, ORCID
- Dmitriy V. Zotov, Anesthesiologist-Intensivist
- Yuliya V. Gusarova, Perfusionist
