Quadricuspid aortic valve
- Authors: Delyagin V.1, Aksyonova N.2
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Affiliations:
- Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology, and Immunology
- City Children’s Polyclinic One Hundred and Fifty
- Issue: Vol 29, No 8 (2018)
- Pages: 48-49
- Section: Articles
- URL: https://journals.eco-vector.com/0236-3054/article/view/117330
- DOI: https://doi.org/10.29296/25877305-2018-08-12
- ID: 117330
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Abstract
A quadricuspid aortic valve (QAV) is a rare congenital heart defect. Ultrasound revealed QAV in a 5-year-old girl with joint hypermobility syndrome who was referred to a cardiologist because of a heart murmur. The concurrence of QAV and connective tissue dysplasia allows one to consider this anomaly as a local manifestation of a genetically determined systemic state.
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About the authors
V. Delyagin
Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology, and Immunology
Email: delyagin-doktor@yandex.ru
Professor
N. Aksyonova
City Children’s Polyclinic One Hundred and Fifty
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