Double jeopardy: long QT3 and Brugada syndromes.

ABSTRACT: 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 mutation.

SUBMITTER: Sandhu A 

PROVIDER: S-EPMC5538234 | biostudies-other | 2017 Aug

REPOSITORIES: biostudies-other