Double jeopardy: long QT3 and Brugada syndromes

Mutations in the SCN5A gene are linked to both the long QT syndrome 3 and Brugada syndrome with few reports describing an overlapping phenotype. We present a unique case and discuss clinical considerations of a patient concurrently exhibiting such conditions with genetic analysis confirming an SCN5A...

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Detalles Bibliográficos
Autores principales: Sandhu, Amneet, Borne, Ryan T., Mam, Chandara, Bunch, T. Jared, Aleong, Ryan G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538234/
https://www.ncbi.nlm.nih.gov/pubmed/28781849
http://dx.doi.org/10.1002/ccr3.1064

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538234/
https://www.ncbi.nlm.nih.gov/pubmed/28781849
http://dx.doi.org/10.1002/ccr3.1064

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