Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Journal of cardiothoracic surgery - 19 Dec 2017

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

Abstract excerpt

BACKGROUND: Congenital long QT syndrome (LQTS) can cause ventricular arrhythmic events with syncope and sudden death resulting from malignant torsades de pointes (TdP) followed by ventricular fibrillations (VFs). However, the syndrome is often overlooked prior to the development of arrhythmic events in patients with congenital heart diseases demonstrating right bundle branch block on electrocardiogram (ECG). We...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Calcium Channels, L-Type
Share to DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Electrocardiography

Share to Genetic Testing

Share to Heart Septal Defects, Atrial

Share to Long QT Syndrome

Share to Ventricular Fibrillation

Source

Open in PubMed Open full text

Identifiers

PMID: 29258620
DOI: 10.1186/s13019-017-0683-4
PMCID: PMC5735880

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Refractory ventricular fibrillations after surgical repair of atrial septal defects in a patient with CACNA1C gene mutation - case report.PMID 29258620Read ↗

Genotype Positive Long QT Syndrome in Patients With Coexisting Congenital Heart Disease.Semantic proximity Read ↗

Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnose.Semantic proximity Read ↗

Dual-loop right atrial tachycardia in a patient post cardiac corrective surgery with inferior vena cava discontinuationSemantic proximity Read ↗

Unroofed Coronary Sinus Without Persistent Left Superior Vena Cava Presenting as an Atrial Septal Defect: A Case ReportSemantic proximity Read ↗

Life-Threatening Ventricular Arrhythmia Induced by Atrial Tachycardia in a Child with an SCN5A Mutation.Semantic proximity Read ↗

Recent advances in managing septal defects: atrial septal defectsSemantic proximity Read ↗

Sudden cardiac arrest during anesthesia in a 30-month-old boy with syndactyly: a case of genetically proven Timothy syndrome.Semantic proximity Read ↗

Pulmonary vein isolation after partial pulmonary vein repair in patient with heterotaxy, anomalous right pulmonary veins and atrial fibrillation with associated cardiomyopathySemantic proximity Read ↗

Genotypic and phenotypic predictors of complete heart block and recovery of conduction after surgical repair of congenital heart disease.Semantic proximity Read ↗

Absence of calcium channel alpha1C-subunit mutation in human atrial fibrillation.Semantic proximity Read ↗

Catheter Ablation of Triggers and Arrhythmogenic Epicardial Substrates in Patients with QT Prolongation.Semantic proximity Read ↗

“Primum non nocere…” Explanting implantable cardioverter-defibrillators in patients with inherited arrhythmia syndromes - Case seriesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.