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Brugada syndrome in infants (<12 months): A case report and literature review
Krishna Kishore Umapathi1, Veronica Godsey2, Hsieh Ting Chang3
1Division of Pediatric Cardiology, Department of Pediatrics, Charleston Area Medical Center, Charleston, West Virginia, USA.
Insights
Infantile Brugada syndrome (BrS) is rare and poorly understood. This case highlights a malignant BrS phenotype in an infant, emphasizing the need for further research into early-onset cardiac conditions.
Area of Science:
- Cardiology
- Pediatric Electrophysiology
- Genetic Cardiology
Background:
- Brugada syndrome (BrS) is typically diagnosed in adults and older children.
- Infantile-onset BrS is rare and lacks comprehensive characterization.
- Early diagnosis and management of BrS in infants remain challenging.
Purpose of the Study:
- To report a case of malignant Brugada syndrome with onset in infancy.
- To review existing literature on infantile-onset BrS.
- To discuss unique features and clinical implications of BrS in this population.
Main Methods:
- Case report of a 7-year-old male with infantile-onset Brugada syndrome.
- Detailed clinical presentation including cardiac arrests due to ventricular tachycardia and fibrillation.
- Comprehensive literature review of infantile-onset Brugada syndrome.
Main Results:
- The patient presented at 8 months of age with a malignant BrS phenotype.
- Multiple episodes of ventricular tachycardia and ventricular fibrillation led to cardiac arrests.
- The patient ultimately succumbed to the condition.
- Literature review identified limited but distinct characteristics of infantile BrS.
Conclusions:
- Malignant Brugada syndrome can manifest in early infancy.
- Infantile-onset BrS presents unique challenges in diagnosis and management.
- Further research is crucial to understand and treat this rare pediatric cardiac condition.
Abstract:
While Brugada syndrome (BrS) is well described in adults and older children, presentation of BrS within the first 12 months of life is rare and therefore poorly characterized. We report a 7-year-old male with a malignant BrS phenotype with onset at 8 months of age, leading to multiple ventricular tachycardia (VT) and ventricular fibrillation (VF) related cardiac arrests and ultimately his death. The report is supplemented by a comprehensive review of existing literature on infantile-onset BrS and unique features in this population are discussed.
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