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

[Clinical manifestations and gene mutation analysis of children with noncompaction of the ventricular myocardium: an analysis of 6 cases].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 1 Jan 2021

Zhang Feng-Hua, An Jin-Dou, Feng Song, Zhang Xiao-Jian, Zhao Xiao-Lin

Abstract excerpt

This article summarizes and analyzes the clinical features and gene mutation characteristics of children with noncompaction of the ventricular myocardium (NVM). For the 6 children with NVM (4 boys and 2 girls), the age of onset ranged from 3 months to 12 years. Of the 6 children, 5 had arrhythmia, 3 had cardiac insufficiency, 1 had poor mental state, and 1 had chest distress and sighing. NVM-related gene...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathies
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Echocardiography

Share to Heart Ventricles

Share to Infant

Share to Mutation

Share to Myocardium

Source

Open in PubMed Open full text

Identifiers

PMID: 33476543
PMCID: PMC7818156

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

[Clinical manifestations and gene mutation analysis of children with noncompaction of the ventricular myocardium: an analysis of 6 cases].PMID 33476543Read ↗

Case Report of Left Ventricular Noncompaction Cardiomyopathy Characterized by Undulating Phenotypes in Adult Patients.Semantic proximity Read ↗

[Phenotype and genotype characteristics of children with cardiomyopathy associated with MYH7 gene mutation: a retrospective analysis].Semantic proximity Read ↗

Noncompaction of the Ventricular Myocardium Is Associated with a De Novo Mutation in the β-Myosin Heavy Chain GeneSemantic proximity Read ↗

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

A case of fetal isolated ventricular noncompaction with TNNT2 gene mutation and literature review.Semantic proximity Read ↗

Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7.Semantic proximity Read ↗

A case report of isolated right ventricular noncompaction with mutation of ACVRL1: a new cause of noncompaction of ventricular myocardium?Semantic proximity Read ↗

Lack of mutations of G4.5 in three families from China with noncompaction of the ventricular myocardium.Semantic proximity Read ↗

Sarcomere mutations in cardiogenesis and ventricular noncompaction.Semantic proximity Read ↗

A novel MYH7 gene mutation in a fetus with left ventricular noncompaction.Semantic proximity Read ↗

Intrafamilial variability of noncompaction of the ventricular myocardium.Semantic proximity Read ↗

Left ventricular noncompaction.Semantic proximity Read ↗

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