Email this article A FAMILIAL CASE OF BRUGADA SYNDROME
- Authors: Avchukhova L.S.1, Salamatina L.V.1, Kolbasin L.N.1, Agapov D.V.1, Urvantseva I.A.1
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Affiliations:
- Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, Surgut
- Issue: Vol 6, No 2 (2012)
- Pages: 64-66
- Section: CASE REPORT
- Published: 16.10.2015
- URL: https://klinitsist.abvpress.ru/Klin/article/view/222
- DOI: https://doi.org/10.17650/1818-8338-2012-6-2-64-66
- ID: 222
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Abstract
The paper describes a familial case of Brugada syndrome type I (genetic variation Y87C) with autosomal-dominant inheritance.
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About the authors
L. S. Avchukhova
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, Surgut
Author for correspondence.
Email: lyudmila85av@mail.ru
Russian Federation
L. V. Salamatina
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, SurgutRussian Federation
L. N. Kolbasin
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, SurgutRussian Federation
D. V. Agapov
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, SurgutRussian Federation
I. A. Urvantseva
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, SurgutRussian Federation
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