27 August 2021>: Articles
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 A* , Bangalore Thimmappa Sanjeev Kumar E , Billal Patel D , Shajil Chalil D , Khalid Abozguia ADOI: 10.12659/AJCR.931535
Am J Case Rep 2021; 22:e931535
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.