Journal ArticleOPEN ACCESS

Double jeopardy: long QT 3 and Brugada syndromes

  • Sandhu A
  • Borne R
  • Mam C
  • et al.
Clinical Case Reports (2017) 5(8) 1315-1319
DOI: 10.1002/ccr3.1064
N/ACitations
Citations of this article
19Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Mutations in the SCN 5A 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 SCN 5A mutation.

Cite

CITATION STYLE

APA

Sandhu, A., Borne, R. T., Mam, C., Bunch, T. J., & Aleong, R. G. (2017). Double jeopardy: long QT 3 and Brugada syndromes. Clinical Case Reports, 5(8), 1315–1319. https://doi.org/10.1002/ccr3.1064

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free