1.
Clin Case Rep
; 5(8): 1315-1319, 2017 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28781849
RESUMO
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.
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