Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.

doi:10.1016/j.jacc.2017.12.019

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

Community

Back to search

Article

Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.

Journal of the American College of Cardiology - 20 Feb 2018

van Waning Jaap I, Caliskan Kadir, Hoedemaekers Yvonne M, van Spaendonck-Zwarts Karin Y, Baas Annette F, Boekholdt S Matthijs, van Melle Joost P, Teske Arco J, Asselbergs Folkert W, Backx Ad P C M, du Marchie Sarvaas Gideon J, Dalinghaus Michiel, Breur Johannes M P J, Linschoten Marijke P M, Verlooij Laura A, Kardys Isabella, Dooijes Dennis, Lekanne Deprez Ronald H, IJpma Arne S, van den Berg Maarten P, Hofstra Robert M W, van Slegtenhorst Marjon A, Jongbloed Jan D H, Majoor-Krakauer Danielle

Abstract excerpt

BACKGROUND: The clinical outcomes of noncompaction cardiomyopathy (NCCM) range from asymptomatic to heart failure, arrhythmias, and sudden cardiac death. Genetics play an important role in NCCM. OBJECTIVES: This study investigated the correlations among genetics, clinical features, and outcomes in adults and children diagnosed with NCCM. METHODS: A retrospective multicenter study from 4 cardiogenetic centers in...

Read the complete abstract on PubMed

Topics

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

Share to Death, Sudden, Cardiac

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Follow-Up Studies

Share to Infant

Share to Infant, Newborn

Share to Isolated Noncompaction of the Ventricular Myocardium

Share to Netherlands

Share to Time Factors

Share to Treatment Outcome

Source

Open in PubMed

Identifiers

PMID: 29447731
DOI: 10.1016/j.jacc.2017.12.019

Genes

MYH7
TTN
MYBPC3

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

Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.PMID 29447731Read ↗

A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction.Semantic proximity Read ↗

Genotype‐Positive Status Is Associated With Poor Prognoses in Patients With Left Ventricular Noncompaction CardiomyopathySemantic proximity Read ↗

Frequency of asymptomatic disease among family members with noncompaction cardiomyopathy.Semantic proximity Read ↗

Genetic Profile of Left Ventricular Noncompaction Cardiomyopathy in Children—A Single Reference Center ExperienceSemantic proximity Read ↗

Genetics and Clinical Features of Noncompaction Cardiomyopathy in the Fetal PopulationSemantic proximity Read ↗

Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologiesSemantic proximity Read ↗

Role of Genetics in Diagnosis and Management of Hypertrophic Cardiomyopathy: A Glimpse into the FutureSemantic proximity Read ↗

Genetic architecture of left ventricular noncompaction in adultsSemantic proximity Read ↗

Multiple genetic variants in adolescent patients with left ventricular noncompaction cardiomyopathy.Semantic proximity Read ↗

Genetic Analysis of Patients with Left Ventricular Noncompaction: Identification of Novel Candidate VariantsSemantic proximity Read ↗

Shared genetic causes of cardiac hypertrophy in children and adults.Semantic proximity Read ↗

[Isolated noncompaction cardiomyopathy with special emphasis on arrhythmia complications].Semantic proximity Read ↗

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