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

Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C): a review of molecular and clinical literature.

Journal of genetic counseling - 1 Aug 2012

Murray Brittney

Abstract excerpt

Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is heritable cardiomyopathy that may result in arrhythmia, heart failure, and sudden cardiac death (SCD). Approximately 50-60% of ARVD/C patient will have an identifiable pathogenic mutation in one of seven genes associated with the cardiac desmosome and other cardiac pathways. Genetic counseling remains complicated, however, because of great...

Read the complete abstract on PubMed

Topics

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

Share to Arrhythmogenic Right Ventricular Dysplasia
Share to Diagnostic Errors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Exercise

Share to SCD gene

Share to Genetic Predisposition to Disease

Share to Genetic Testing

Share to Risk Factors

Share to Signal Transduction

Source

Identifiers

PMID: 22426942
DOI: 10.1007/s10897-012-9497-7

Genes

SCD

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

Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C): a review of molecular and clinical literature.PMID 22426942Read ↗

Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update.Semantic proximity Read ↗

Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a not so rare "disease of the desmosome" with multiple clinical presentations.Semantic proximity Read ↗

Arrhythmogenic right ventricular cardiomyopathy: an update on pathophysiology, genetics, diagnosis, and risk stratification.Semantic proximity Read ↗

Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy – Three Decades of Progress –Semantic proximity Read ↗

Diagnostic and therapeutic strategies for arrhythmogenic right ventricular dysplasia/cardiomyopathy patient.Semantic proximity Read ↗

Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy.Semantic proximity Read ↗

Arrhythmogenic Right Ventricular Cardiomyopathy: Progress Toward Personalized Management.Semantic proximity Read ↗

Arrhythmogenic cardiomyopathy: etiology, diagnosis, and treatment.Semantic proximity Read ↗

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

Arrhythmogenic right ventricular cardiomyopathy, clinical manifestations, and diagnosis.Semantic proximity Read ↗

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria.Semantic proximity Read ↗

Arrhythmogenic Cardiomyopathy.Semantic proximity Read ↗

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