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A case report of a young patient with both Brugada and long QT3 syndrome: between the hammer and the anvil
BACKGROUND: Brugada syndrome (BrS) is an inherited disorder associated with increased risk of ventricular arrhythmias and sudden cardiac death. The most common genetic alteration is a loss of function mutation of SCN5A gene. Several mutations in SCN5A gene were found to be associated with an overlap...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543550/ https://www.ncbi.nlm.nih.gov/pubmed/34708182 http://dx.doi.org/10.1093/ehjcr/ytab053 |