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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...
Kaydedildi:
| Yayımlandı: | Ann Noninvasive Electrocardiol |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
John Wiley and Sons Inc.
2017
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| Konular: | |
| Online Erişim: | 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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