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

An adolescent with possible arrhythmogenic right ventricular dysplasia and long QT syndrome: evaluation and management.

Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc - 1 Jan 2013

Tisma-Dupanovic Svjetlana, Wagner Jonathan B, Shah Sanket, Huang David T, Moss Arthur J

Abstract excerpt

We describe a unique presentation of arrhythmogenic right ventricular dysplasia (ARVD) in a 14-year-old Caucasian male who was additionally diagnosed with long QT syndrome (LQTS). Genetic testing eventually confirmed the diagnosis of both ARVD and LQTS, which combined, to our knowledge, has not been reported in the literature.

Read the complete abstract on PubMed

Topics

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

Share to Adrenergic beta-Antagonists
Share to Arrhythmogenic Right Ventricular Dysplasia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cardiac Catheterization

Share to Catheter Ablation

Share to Echocardiography

Share to Electrocardiography

Share to Exercise Test

Share to Long QT Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 23347029
DOI: 10.1111/anec.12043
PMCID: PMC6932431

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

An adolescent with possible arrhythmogenic right ventricular dysplasia and long QT syndrome: evaluation and management.PMID 23347029Read ↗

Arrhythmogenic Right Ventricular Cardiomyopathy in Pediatric Patients: An Important but Underrecognized Clinical EntitySemantic proximity Read ↗

Arrhythmogenic right ventricular dysplasia/cardiomyopathy: clinical profile of four patients and review.Semantic proximity Read ↗

Arrhythmogenic Right Ventricular Dysplasia: An Under-recognized Form of Inherited Cardiomyopathy.Semantic proximity Read ↗

Clinical Diagnosis, Imaging, and Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy/DysplasiaSemantic proximity Read ↗

Diagnosing ARVC in Pediatric Patients Applying the Revised Task Force Criteria: Importance of Imaging, 12-Lead ECG, and Genetics.Semantic proximity Read ↗

Arrhythmogenic right ventricular dysplasia.Semantic proximity Read ↗

Arrhythmogenic right ventricular dysplasia: from genetics to treatment.Semantic proximity Read ↗

Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome.Semantic proximity Read ↗

Arrhythmogenic right-ventricular dysplasia/cardiomyopathy.Semantic proximity Read ↗

Desmoplakin Cardiomyopathy in Pediatric Patients: A Distinct, Underrecognized Cohort of Arrhythmogenic Cardiomyopathy.Semantic proximity Read ↗

An updated review on the clinicopathologic aspects of arrhythmogenic right ventricular cardiomyopathy.Semantic proximity Read ↗

Cardiac phenotype and long-term prognosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia patients with late presentation.Semantic proximity Read ↗

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