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Late‐onset severe long QT syndrome
We report a case of torsades de pointes arrhythmia as the first manifestation of congenital Long QT syndrome in a 77‐year‐old man with family history of sudden unexplained death. This case illustrates the importance of vigilant clinical assessment and genetic counseling in families with sudden death...
Enregistré dans:
| Publié dans: | Ann Noninvasive Electrocardiol |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
John Wiley and Sons Inc.
2017
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6931632/ https://ncbi.nlm.nih.gov/pubmed/29194874 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/anec.12517 |
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