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: 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 ^A

DOI: 10.12659/AJCR.931535

Am J Case Rep 2021; 22:e931535

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Background Case Report Discussion Conclusions References:

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Figure 2. Computed tomography coronary angiogram. (A) Absence of take-off of the RCA from the right coronary sinus of Valsalva (yellow arrow) and normal origin of the LMS which bifurcates into the LAD and LCx (white arrows). (B) Course of the LCx on the posterior atrioventricular groove and continuation of its course in the RCA territory along with take-off of the posterior descending artery. LAD – left anterior descending artery; LCx – left circumflex artery; LMS – left main stem artery; RCA – right coronary artery.

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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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