A clinical case of arrhythmogenic right ventricular dysplasia
https://doi.org/10.21886/2712-8156-2021-2-1-109-114
Abstract
Arhythmogenic right ventricular dysplasia (ADP) refers to hereditary myocardial diseases, in which there are structural and functional disorders in the right ventricular myocardium, causing rhythm and conduction disorders, including fatal ventricular arrhythmias. ADP is considered one of the most common causes of sudden cardiac death in young people and people who are engaged in sports. However, in practice, there are cases of this disease in people of an older age category. Diagnosis of ADP is still difficult due to the possible long-term asymptomatic course of the disease. The article describes a clinical case of ADP in a 48-year-old man.
About the Authors
E. V. Solovyoval
Privolzhsky Research Medical University
Russian Federation
Russian Federation
Elena V. Solovyova, Cand. Sci. (Med.), Associate Professor.
Nizhny Novgorod
N. A. Popova
Privolzhsky Research Medical University
Russian Federation
Russian Federation
Natalia A. Popova, Cand. Sci. (Med.), Associate Professor.
Nizhny Novgorod
T. V. Vlasoval
Privolzhsky Research Medical University
Russian Federation
Russian Federation
Tatyana V. Vlasova, Cand. Sci. (Med.), Associate Professor.
Nizhny Novgorod
M. L. Gorbunova
Clinic of modern technologies Sadko Nizhny Novgorod
Russian Federation
Russian Federation
Marina L. Gorbunova, Cand. Sci. (Med.), Associate Professor, Cardiologist.
Nizhny Novgorod
L. N. Antsygina
B.A. Korolev Specialized Cardiosurgical Clinical Hospital
Russian Federation
Russian Federation
Lyudmila N. Antsygina, Cand. Sci. (Med.), Cardiologist.
Nizhny Novgorod
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Review
For citations:
Solovyoval E.V., Popova N.A., Vlasoval T.V., Gorbunova M.L., Antsygina L.N. A clinical case of arrhythmogenic right ventricular dysplasia. South Russian Journal of Therapeutic Practice. 2021;2(1):109-114. (In Russ.) https://doi.org/10.21886/2712-8156-2021-2-1-109-114
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