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Brugada syndrome with a novel missense mutation in SCN5A gene: A case report from Bangladesh
Brugada syndrome is an inherited cardiac arrhythmia that follows autosomal dominant transmission and can cause sudden death. We report a case of Brugada syndrome in a 55-year-old male patient presented with recurrent palpitation, atypical chest pain and presyncope. ECG changes were consistent with t...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Elsevier
2014
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3946469/ https://ncbi.nlm.nih.gov/pubmed/24581105 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ihj.2013.12.003 |
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