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A typical, relapsing case of Brugada Syndrome
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  • Erick Alexanderson-Rosas,
  • Mariell Alejandra Rodríguez-Salazar,
  • Pamela Rosario Morales-Álvarez,
  • Gerardo Zavala-García,
  • Rubén Alejandro León-Laredo,
  • Jonas Heli Flores-Peralta,
  • Jethro Singer-de-la-Garza,
  • Alejandro Bautista-Pérez-Gavilán,
  • Leonardo Proaño-Bernal
Erick Alexanderson-Rosas
Instituto Nacional de Cardiologia Ignacio Chavez

Corresponding Author:ealexanderson.edu@gmail.com

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Mariell Alejandra Rodríguez-Salazar
Instituto Nacional de Cardiologia Ignacio Chavez
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Pamela Rosario Morales-Álvarez
Instituto Nacional de Cardiologia Ignacio Chavez
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Gerardo Zavala-García
Instituto Nacional de Cardiologia Ignacio Chavez
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Rubén Alejandro León-Laredo
Universidad Anahuac Mexico
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Jonas Heli Flores-Peralta
Universidad Nacional Autonoma de Mexico
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Jethro Singer-de-la-Garza
Universidad Nacional Autonoma de Mexico
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Alejandro Bautista-Pérez-Gavilán
Instituto Nacional de Cardiologia Ignacio Chavez
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Leonardo Proaño-Bernal
Instituto Nacional de Cardiologia Ignacio Chavez
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Abstract

Introduction: Brugada syndrome (BrS) is a primary electrical disorder that has been a subject of study because of its association with cases of sudden cardiac death (SCD). Methods: This article presents a case of a 32-year-old man with no prior cardiovascular disease history who experienced syncope and exhibited electrocardiographic changes. Results: An ajmaline test was performed, which revealed the presence of type II and I Brugada patterns. A literature review was conducted, covering the definition, classification, pathophysiology, genetics, prognosis, and treatment of this condition. Conclusion: Identifying electrocardiographic patterns and taking a correct clinical history can guide a timely therapeutic approach.