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 cardiomyopathy.

Orphanet journal of rare diseases - 2 Apr 2016

Pilichou Kalliopi, Thiene Gaetano, Bauce Barbara, Rigato Ilaria, Lazzarini Elisabetta, Migliore Federico, Perazzolo Marra Martina, Rizzo Stefania, Zorzi Alessandro, Daliento Luciano, Corrado Domenico, Basso Cristina

Abstract excerpt

Arrhythmogenic cardiomyopathy (AC) is a heart muscle disease clinically characterized by life-threatening ventricular arrhythmias and pathologically by an acquired and progressive dystrophy of the ventricular myocardium with fibro-fatty replacement. Due to an estimated prevalence of 1:2000-1:5000, AC is listed among rare diseases. A familial background consistent with an autosomal-dominant trait of inheritance is...

Read the complete abstract on PubMed

Topics

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

Share to Arrhythmias, Cardiac
Share to beta Catenin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cardiomyopathies

Share to Cardiovascular Effects of Exercise

Share to Heterozygote

Share to Mutation

Share to Sports injuries and prevention

Source

Open in PubMed Open full text

Identifiers

PMID: 27038780
DOI: 10.1186/s13023-016-0407-1
PMCID: PMC4818879

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 cardiomyopathy.PMID 27038780Read ↗

Arrhythmogenic Cardiomyopathy.Semantic proximity Read ↗

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

Arrhythmogenic cardiomyopathy: advances in diagnosis and disease pathogenesis.Semantic proximity Read ↗

Pathophysiology of arrhythmogenic cardiomyopathy.Semantic proximity Read ↗

Arrhythmogenic Left Ventricular Cardiomyopathy: Genotype-Phenotype Correlations and New Diagnostic CriteriaSemantic proximity Read ↗

The Many Faces of Arrhythmogenic Cardiomyopathy: An OverviewSemantic proximity Read ↗

Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis.Semantic proximity Read ↗

Arrhythmogenic cardiomyopathy: pathogenesis, pro-arrhythmic remodelling, and novel approaches for risk stratification and therapy.Semantic proximity Read ↗

Arrhythmogenic cardiomyopathy: An in-depth look at molecular mechanisms and clinical correlatesSemantic proximity Read ↗

Differential diagnosis of arrhythmogenic cardiomyopathy: phenocopies versus disease variants.Semantic proximity Read ↗

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

Arrhythmogenic Right Ventricular Cardiomyopathy: A Comprehensive ReviewSemantic proximity Read ↗

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