| Literature DB >> 24620847 |
Emiliana Franco1, Andre Dias, Daniele Teresa, Kathy Hebert.
Abstract
Brugada Syndrome (BrS) is a cardiac disorder characterized by incomplete right bundle-branch block and ST elevations in the anterior precordial leads especially V1 -V3 , associated with an increased risk for sudden cardiac death (SCD) in young adults. Our case describes a patient with family history of sudden infant death syndrome (SIDS) who presented with a Brugada pattern unmasked by severe hyperkalemia and diabetic ketoacidosis. Several studies have concluded there may be a genetic link among SIDS, SDC, and BrS resulting from mutations in cardiac ion channel-related genes. Recognizing SIDS as part of the diagnostic criteria for BrS would help us identifying a significant number of families susceptible to develop SCD (as well as SIDS). ©2013 Wiley Periodicals, Inc.Entities:
Keywords: Electrophysiology-Brugada syndrome; clinical; clinical, electrophysiology-cardiac arrest/sudden death
Mesh:
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Year: 2013 PMID: 24620847 PMCID: PMC6932589 DOI: 10.1111/anec.12086
Source DB: PubMed Journal: Ann Noninvasive Electrocardiol ISSN: 1082-720X Impact factor: 1.468