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...

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Detalles Bibliográficos
Autores principales: Mondal, Tapas, Sullivan, Kristen, Divakaramenon, Syam, Hamilton, Robert M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793134/
https://www.ncbi.nlm.nih.gov/pubmed/33442618
http://dx.doi.org/10.1093/ehjcr/ytaa336

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793134/
https://www.ncbi.nlm.nih.gov/pubmed/33442618
http://dx.doi.org/10.1093/ehjcr/ytaa336

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