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Antiepileptic rufinamide and QTc interval shortening in a patient with long QT syndrome: case report
BACKGROUND: There is limited pharmacologic therapy to reduce the QT interval in hereditary long QT syndrome (LQTS). CASE SUMMARY: We describe a child with Allan–Herndon–Dudley syndrome, Lennox–Gastaut epileptic syndrome (LGS), and LQTS Type 1 (LQTS1). Rufinamide was added to his antiepileptic medica...
Tallennettuna:
| Julkaisussa: | Eur Heart J Case Rep |
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| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7793134/ https://ncbi.nlm.nih.gov/pubmed/33442618 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ehjcr/ytaa336 |
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