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

Patient: Female, 59-year-old Final Diagnosis: Absence of right coronary artery • patent foramen ovale • positive for Brugada-related gene variant Symptoms: Angina Medication:— Clinical Procedure: — Specialty: Cardiology OBJECTIVE: Rare coexistence of disease or pathology BACKGROUND: Brugada syndrome...

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Detalles Bibliográficos
Autores principales: Katsaras, Dimitrios, Kumar, Bangalore Thimmappa Sanjeev, Patel, Billal, Chalil, Shajil, Abozguia, Khalid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409454/
https://www.ncbi.nlm.nih.gov/pubmed/34446689
http://dx.doi.org/10.12659/AJCR.931535

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409454/
https://www.ncbi.nlm.nih.gov/pubmed/34446689
http://dx.doi.org/10.12659/AJCR.931535

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