A 59-Year-Old Woman with Familial Brugada Syndrome and the c.664C>T Variant of the Sodium Voltage-Gated Channel Alpha Subunit 5 (SCN5A) Gene, Accompanied by Congenital Absence of the Right Coronary Artery, Patent Foramen Ovale, and Ischemic Stroke

Dimitrios Katsaras; Bangalore Thimmappa Sanjeev Kumar; Billal Patel; Shajil Chalil; Khalid Abozguia

doi:10.12659/AJCR.931535

27 August 2021 : Case report United Kingdom

A 59-Year-Old Woman with Familial Brugada Syndrome and the c.664C>T Variant of the Sodium Voltage-Gated Channel Alpha Subunit 5 (SCN5A) Gene, Accompanied by Congenital Absence of the Right Coronary Artery, Patent Foramen Ovale, and Ischemic Stroke

Rare coexistence of disease or pathology

Dimitrios Katsaras^1ABCDEF*, Bangalore Thimmappa Sanjeev Kumar^2E, Billal Patel^1DEF, Shajil Chalil^1DEG, Khalid Abozguia^1ADEFG

DOI: 10.12659/AJCR.931535

Am J Case Rep 2021; 22:e931535

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Figure 1. Baseline ECG. Baseline ECG shows sinus rhythm with nonspecific repolarization abnormalities in the form of T wave inversion in leads V1–V3 with no features suggestive of type 1 Brugada syndrome.

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A 59-Year-Old Woman with Familial Brugada Syndrome and the c.664C>T Variant of the Sodium Voltage-Gated Channel Alpha Subunit 5 (SCN5A) Gene, Accompanied by Congenital Absence of the Right Coronary Artery, Patent Foramen Ovale, and Ischemic Stroke

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