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Rarity and phenotypic heterogeneity provide challenges in the diagnosis of Andersen-Tawil syndrome: Two cases presenting with ECGs mimicking catecholaminergic polymorphic ventricular tachycardia (CPVT).
Tully, I; Atherton, J; Hunt, L; Ingles, J; Semsarian, C; McGaughran, J.
Affiliation
  • Tully I; Genetic Health Queensland, Royal Brisbane & Women's Hospital, Australia; All Wales Medical Genetic Service, University Hospital of Wales, Cardiff, UK. Electronic address: ian.tully2@wales.nhs.uk.
  • Atherton J; Department of Cardiology, Royal Brisbane & Women's Hospital, Australia.
  • Hunt L; Genetic Health Queensland, Royal Brisbane & Women's Hospital, Australia.
  • Ingles J; Centenary Institute, University of Sydney, Australia.
  • Semsarian C; Centenary Institute, University of Sydney, Australia.
  • McGaughran J; Genetic Health Queensland, Royal Brisbane & Women's Hospital, Australia.
Int J Cardiol ; 201: 473-5, 2015 Dec 15.
Article in En | MEDLINE | ID: mdl-26322597
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tachycardia, Ventricular / Andersen Syndrome Type of study: Diagnostic_studies Limits: Adult / Child / Female / Humans Language: En Journal: Int J Cardiol Year: 2015 Document type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tachycardia, Ventricular / Andersen Syndrome Type of study: Diagnostic_studies Limits: Adult / Child / Female / Humans Language: En Journal: Int J Cardiol Year: 2015 Document type: Article