A clinical case of a combination of Ebstein’s anomaly and genetically determined cardiomyopathy in a child who required a heart transplantation in childhood
https://doi.org/10.18705/2782-3806-2023-3-2139-147
Abstract
The article presents a rare case of a combination of Ebstein’s anomaly and primary cardiomyopathy in a 14-year-old teenager. The clinical case demonstrates diagnostic difficulties due to an unusual clinical picture, as well as difficulties in interpretation and choice of treatment tactics.
Supporting agencies: The study was carried out with the financial support of the Ministry of Science and Higher Education of the Russian Federation (Agreement No. 075-15-2022301 dated 04/20/2022)
About the Authors
E. S. Vasichkina
Almazov National Medical Research Centre
Russian Federation
Russian Federation
Vasichkina Elena S. - PhD, MD, Head of the Scientific Research Centre for Unknown, Rare and Genetically Caused Diseases of the World-Class Research Centre for Personalized Medicine, Professor of the Department of Pediatric Diseases of the Medical Faculty of the Institute of Medical Education.
Saint Petersburg
T. L. Vershinina
Almazov National Medical Research Centre
Russian Federation
Russian Federation
Vershinina Tatiana L. - head of the Department of Pediatric Cardiology and Medical Rehabilitation, cardiologist, Children’s medical and rehabilitation complex.
Saint Petersburg
A. A. Morozov
Almazov National Medical Research Centre
Russian Federation
Russian Federation
Morozov Aleksandr A. - CM, Cardiac Surgeon of the Department of Pediatric Cardiac Surgery.
Saint Petersburg
P. A. Fedotov
Almazov National Medical Research Centre
Russian Federation
Russian Federation
Fedotov Petr A. - Head of the Research Laboratory of High-Tech Methods for the Treatment of Heart Failure, Associate Professor of the Department of Cardiology.
Saint Petersburg
T. S. Kovalchuk
Almazov National Medical Research Centre
Russian Federation
Russian Federation
Kovalchuk Tatiana S. - junior researcher at the Research Institute of Unknown, Rare and Genetically Determined Diseases of the World-Class Research Centre for Personalized Medicine, pediatric cardiologist of the Pediatric Cardiology and Medical Rehabilitation Department.
Saint Petersburg
D. Yu. Alekseeva
Almazov National Medical Research Centre
Russian Federation
Russian Federation
Alekseeva Darya Yu. - СM, Researcher, Research Institute of Unknown, Rare and Genetically Caused Diseases, World-Class Research Centre for Personalized Medicine.
Akkuratova str., 2, Saint Petersburg, 197341
E. V. Grekhov
Almazov National Medical Research Centre
Russian Federation
Russian Federation
Grekhov Evgeniy V. - CM, Head of the Scientific Research Group of Pediatric Cardiac Surgery, Research Institute of Cardiovascular Diseases in Children.
Saint Petersburg
T. M. Pervunina
Almazov National Medical Research Centre
Russian Federation
Russian Federation
Pervunina Tatiana M. - PhD, MD, director of the Institute of Perinatology and Pediatrics, leading researcher of the Research Institute of Unknown, Rare and Genetically Determined Diseases of the World-Class Research Centre for Personalized Medicine, pediatrician of the highest category.
Saint Petersburg
References
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Review
For citations:
Vasichkina E.S., Vershinina T.L., Morozov A.A., Fedotov P.A., Kovalchuk T.S., Alekseeva D.Yu., Grekhov E.V., Pervunina T.M. A clinical case of a combination of Ebstein’s anomaly and genetically determined cardiomyopathy in a child who required a heart transplantation in childhood. Russian Journal for Personalized Medicine. 2023;3(2):139-147. (In Russ.) https://doi.org/10.18705/2782-3806-2023-3-2139-147
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