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Congenital long QT syndrome aggravated by salt-wasting nephropathy
Long QT syndrome (LQTS) is characterized by episodes of fainting or by sudden death as a result of torsades de pointes (TdP). In both the congenital and acquired forms of the syndrome, symptoms often become manifest upon exposure to additional clinical stressors of repolarization, such as drugs or h...
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| Auteurs principaux: | , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2005
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1350445/ https://ncbi.nlm.nih.gov/pubmed/15851323 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2004.11.015 |
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