Literature DB >> 26768964

Compound Heterozygous Triadin Mutation Causing Cardiac Arrest in Two Siblings.

Mark A Walsh1,2, Alan G Stuart1,2, Helene B Schlecht3, Andrew F James4, Jules C Hancox4, Ruth A Newbury-Ecob5.   

Abstract

We present the case of two siblings who both presented with an out-of-hospital cardiac arrest at 2 years of age. Both siblings underwent internal cardiac defibrillator implantation and both had recurrent episodes of ventricular fibrillation (VF). A compound heterozygous mutation in the triadin gene was discovered; one of these mutations has been described previously in the homozygous state, and the other one is unreported. The combination of these mutations has resulted in a particularly arrhythmogenic phenotype, with cardiac arrest occurring at a very young age and recurrent episodes of VF despite β-blockade. Flecainide seems to have been very effective in preventing clinical arrhythmias for this particular mutation. ©2016 Crown Copyright and Wiley Periodicals, Inc. Pacing and Clinical Electrophysiology
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  CPVT; cardiac arrest; pediatrics; triadin; ventricular fibrillation

Mesh:

Substances:

Year:  2016        PMID: 26768964     DOI: 10.1111/pace.12813

Source DB:  PubMed          Journal:  Pacing Clin Electrophysiol        ISSN: 0147-8389            Impact factor:   1.976


  5 in total

1.  Interplay between Triadin and Calsequestrin in the Pathogenesis of CPVT in the Mouse.

Authors:  Marine Cacheux; Jérémy Fauconnier; Jérôme Thireau; Alexis Osseni; Jacques Brocard; Nathalie Roux-Buisson; Julie Brocard; Julien Fauré; Alain Lacampagne; Isabelle Marty
Journal:  Mol Ther       Date:  2019-09-13       Impact factor: 11.454

2.  Congenital myopathy associated with the triadin knockout syndrome.

Authors:  Andrew G Engel; Keeley R Redhage; David J Tester; Michael J Ackerman; Duygu Selcen
Journal:  Neurology       Date:  2017-02-15       Impact factor: 9.910

Review 3.  The Genetics and Epigenetics of Ventricular Arrhythmias in Patients Without Structural Heart Disease.

Authors:  Mengru Wang; Xin Tu
Journal:  Front Cardiovasc Med       Date:  2022-06-15

Review 4.  Excitation-Contraction Coupling Alterations in Myopathies.

Authors:  Isabelle Marty; Julien Fauré
Journal:  J Neuromuscul Dis       Date:  2016-11-29

5.  A unique triadin exon deletion causing a null phenotype.

Authors:  Barry M O'Callaghan; Jules C Hancox; Alan G Stuart; Catherine Armstrong; Maggie M Williams; Alison Hills; Hazel Pearce; Carolyn L Dent; Mary Gable; Mark A Walsh
Journal:  HeartRhythm Case Rep       Date:  2018-08-04
  5 in total

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