Literature DB >> 20395683

Sick sinus syndrome, progressive cardiac conduction disease, atrial flutter and ventricular tachycardia caused by a novel SCN5A mutation.

Anders G Holst1, Bo Liang, Thomas Jespersen, Henning Bundgaard, Stig Haunso, Jesper Hastrup Svendsen, Jacob Tfelt-Hansen.   

Abstract

Mutations in the cardiac sodium channel encoded by the gene SCN5A can result in a wide array of phenotypes. We report a case of a young male with a novel SCN5A mutation (R121W) afflicted by sick sinus syndrome, progressive cardiac conduction disorder, atrial flutter and ventricular tachycardia. His father carried the same mutation, but had a milder phenotype, presenting with progressive cardiac conduction later in life. The mutation was found to result in a loss-of-function in the sodium current. In conclusion, the same SCN5A mutation can result in a wide array of clinical phenotypes and perhaps the spectrum of SCN5A loss-of-function associated disease entities should be viewed as one syndrome. Copyright (c) 2010 S. Karger AG, Basel.

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Year:  2010        PMID: 20395683     DOI: 10.1159/000312747

Source DB:  PubMed          Journal:  Cardiology        ISSN: 0008-6312            Impact factor:   1.869


  11 in total

1.  Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 α-subunits.

Authors:  Jérôme Clatot; Azza Ziyadeh-Isleem; Svetlana Maugenre; Isabelle Denjoy; Haiyan Liu; Gilles Dilanian; Stéphane N Hatem; Isabelle Deschênes; Alain Coulombe; Pascale Guicheney; Nathalie Neyroud
Journal:  Cardiovasc Res       Date:  2012-06-27       Impact factor: 10.787

2.  Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.

Authors:  Jared W Magnani; Jennifer A Brody; Bram P Prins; Dan E Arking; Honghuang Lin; Xiaoyan Yin; Ching-Ti Liu; Alanna C Morrison; Feng Zhang; Tim D Spector; Alvaro Alonso; Joshua C Bis; Susan R Heckbert; Thomas Lumley; Colleen M Sitlani; L Adrienne Cupples; Steven A Lubitz; Elsayed Z Soliman; Sara L Pulit; Christopher Newton-Cheh; Christopher J O'Donnell; Patrick T Ellinor; Emelia J Benjamin; Donna M Muzny; Richard A Gibbs; Jireh Santibanez; Herman A Taylor; Jerome I Rotter; Leslie A Lange; Bruce M Psaty; Rebecca Jackson; Stephen S Rich; Eric Boerwinkle; Yalda Jamshidi; Nona Sotoodehnia
Journal:  Circ Cardiovasc Genet       Date:  2014-06

Review 3.  The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunction.

Authors:  Raffaella Milanesi; Annalisa Bucchi; Mirko Baruscotti
Journal:  J Interv Card Electrophysiol       Date:  2015-04-12       Impact factor: 1.900

4.  Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.

Authors:  Elisabet Selga; Oscar Campuzano; Mel Lina Pinsach-Abuin; Alexandra Pérez-Serra; Irene Mademont-Soler; Helena Riuró; Ferran Picó; Mònica Coll; Anna Iglesias; Sara Pagans; Georgia Sarquella-Brugada; Paola Berne; Begoña Benito; Josep Brugada; José M Porres; Matilde López Zea; Víctor Castro-Urda; Ignacio Fernández-Lozano; Ramon Brugada
Journal:  PLoS One       Date:  2015-07-14       Impact factor: 3.240

Review 5.  Atrial arrhythmias in inherited arrhythmogenic disorders.

Authors:  Can Hasdemir
Journal:  J Arrhythm       Date:  2016-02-09

6.  Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutation.

Authors:  Hisaaki Aoki; Yoshihide Nakamura; Seiko Ohno; Takeru Makiyama; Minoru Horie
Journal:  J Arrhythm       Date:  2016-07-02

7.  Mutations in NaV1.5 Reveal Calcium-Calmodulin Regulation of Sodium Channel.

Authors:  Eyal Nof; Leonid Vysochek; Eshcar Meisel; Elena Burashnikov; Charles Antzelevitch; Jerome Clatot; Roy Beinart; David Luria; Michael Glikson; Shimrit Oz
Journal:  Front Physiol       Date:  2019-06-05       Impact factor: 4.566

Review 8.  Genetic Complexity of Sinoatrial Node Dysfunction.

Authors:  Michael J Wallace; Mona El Refaey; Pietro Mesirca; Thomas J Hund; Matteo E Mangoni; Peter J Mohler
Journal:  Front Genet       Date:  2021-04-01       Impact factor: 4.599

9.  Phosphorylation of Lamin A/C at serine 22 modulates Nav 1.5 function.

Authors:  Michael A Olaopa; Tomohiko Ai; Bo Chao; Xiangshu Xiao; Matteo Vatta; Beth A Habecker
Journal:  Physiol Rep       Date:  2021-11

10.  Reevaluating the Mutation Classification in Genetic Studies of Bradycardia Using ACMG/AMP Variant Classification Framework.

Authors:  Liting Cheng; Xiaoyan Li; Lin Zhao; Zefeng Wang; Junmeng Zhang; Zhuo Liang; Yongquan Wu
Journal:  Int J Genomics       Date:  2020-02-25       Impact factor: 2.326

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