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Article

Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.

Archives of cardiovascular diseases - 1 Dec 2013

Wahbi Karim, Algalarrondo Vincent, Bécane Henri Marc, Fressart Véronique, Beldjord Chérif, Azibi Kamel, Lazarus Arnaud, Berber Nawal, Radvanyi-Hoffman Hélène, Stojkovic Tanya, Béhin Anthony, Laforêt Pascal, Eymard Bruno, Hatem Stéphane, Duboc Denis

Abstract excerpt

BACKGROUND: In patients with myotonic dystrophy type 1 (DM1), the mechanisms underlying sudden cardiac death, which occurs in up to 1/3 of patients, are unclear. AIMS: To study the potential role of Brugada syndrome in ventricular tachyarrhythmias and sudden death in DM1 patients. METHODS: We screened 914 adult patients included in the DM1 Heart Registry during 2000-2009 for the presence of type 1 Brugada pattern...

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Identifiers

PMID: 24140416
DOI: 10.1016/j.acvd.2013.08.003

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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