A FAMILIAL CASE OF BRUGADA SYNDROME
https://doi.org/10.17650/1818-8338-2012-6-2-64-66
Abstract
The paper describes a familial case of Brugada syndrome type I (genetic variation Y87C) with autosomal-dominant inheritance.
About the Authors
L. S. Avchukhova
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, Surgut
Russian Federation
Russian Federation
L. V. Salamatina
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, Surgut
Russian Federation
Russian Federation
L. N. Kolbasin
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, Surgut
Russian Federation
Russian Federation
D. V. Agapov
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, Surgut
Russian Federation
Russian Federation
I. A. Urvantseva
Center for Diagnosis and Cardiovascular Surgery, District Cardiology Dispensary, Khanty-Mansi Autonomous District-Yugra, Surgut
Russian Federation
Russian Federation
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Review
For citations:
Avchukhova L.S., Salamatina L.V., Kolbasin L.N., Agapov D.V., Urvantseva I.A. A FAMILIAL CASE OF BRUGADA SYNDROME. The Clinician. 2012;6(2):64-66. (In Russ.) https://doi.org/10.17650/1818-8338-2012-6-2-64-66
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