Unknown

Dataset Information

0

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

Similar Datasets

| S-EPMC4737709 | biostudies-literature
| S-EPMC9272763 | biostudies-literature
| S-EPMC6788474 | biostudies-literature
| S-EPMC3288170 | biostudies-literature
| S-EPMC7332759 | biostudies-literature
| S-EPMC1592481 | biostudies-literature
| S-EPMC6197104 | biostudies-literature
| S-EPMC5063259 | biostudies-literature
2020-02-22 | GSE145733 | GEO
| S-EPMC1997279 | biostudies-literature