Refractory ventricular fibrillations after surgical repair of atrial septal defects in a patient with CACNA1C gene mutation

Refractory ventricular fibrillations after surgical repair of atrial septal defects in a patient with CACNA1C gene mutation - case report

Published:2017-12 Issue:1 Volume:12 Page:
ISSN:1749-8090
Container-title:Journal of Cardiothoracic Surgery
language:en
Short-container-title:J Cardiothorac Surg

Author:

Kojima Ai,Shikata Fumiaki^ORCID,Okamura Toru,Higaki Takashi,Ohno Seiko,Horie Minoru,Uchita Shunji,Kawanishi Yujiro,Namiguchi Kenji,Yasugi Takumi,Izutani Hironori

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,General Medicine,Surgery,Pulmonary and Respiratory Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13019-017-0683-4.pdf

Reference15 articles.

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2. Walls J, Sanatani S, Hamilton R. Post-hoc diagnosis of congenital long qt syndrome in patients with tetralogy of fallot. Pediatr Cardiol. 2005;26:107–10.

3. Krasner BS, Girdwood R, Smith H. The effect of slow releasing oral magnesium chloride on the qtc interval of the electrocardiogram during open heart surgery. Can Anaesth Soc J. 1981;28:329–33.

4. Kim SJ, Pundi KN, Bos JM, Ackerman MJ. Ventricular fibrillation after elective surgery in an adolescent with long qt syndrome. BMJ Case Reports. 2015. doi: 10.1136/bcr-2015-212365 .

5. Fukuyama M, Wang Q, Kato K, Ohno S, Ding WG, Toyoda F, et al. Long qt syndrome type 8: novel cacna1c mutations causing qt prolongation and variant phenotypes. Europace. 2014;16:1828–37.

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1. Geno- and phenotypic characteristics and clinical outcomes of CACNA1C gene mutation associated Timothy syndrome, “cardiac only” Timothy syndrome and isolated long QT syndrome 8: A systematic review;Frontiers in Cardiovascular Medicine;2022-11-29

2. Electrical storm after correction of an uncomplicated congenital atrial septal defect in an adult: a case report;BMC Cardiovascular Disorders;2021-07-22

3. Penetrance and expressivity of the R858HCACNA1Cvariant in a five-generation pedigree segregating an arrhythmogenic channelopathy;Molecular Genetics & Genomic Medicine;2018-10-21