Left Ventricular Noncompaction Lvnc | List of Frontiers open access articles

Case Report

Published on 04 Aug 2022

Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report

in Pediatric Cardiology

Thomas Caiffa
Antimo Tessitore
Loira Leoni
Elena Reffo
Daniela Chicco
Biancamaria D'Agata Mottolese
Elisa Rubinato
Giorgia Girotto
Stefania Lenarduzzi
Egidio Barbi

Frontiers in Pediatrics

doi 10.3389/fped.2022.970240

3,391 views
5 citations

Case Report

Published on 14 Sep 2023

Case report: A rare case of left ventricular noncompaction in two Chinese siblings with becker muscular dystrophy caused by deletion of exons 10 to 12 in the DMD gene

in Cardiovascular Genetics and Systems Medicine

Jingdong Li
Wanyue Zhu
Guanhua Su
Feng Zhu
Xinxin Shuai
Yidi Meng
Jiaming Zhang
Hao Chen

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1243825

2,618 views

Case Report

Published on 24 Feb 2022

Case Report: Biventricular Noncompaction Cardiomyopathy With Pulmonary Stenosis and Bradycardia in a Fetus With KCNH2 Mutation

in Genetics of Common and Rare Diseases

Hairui Sun
Xiaowei Liu
Xiaoyan Hao
Xiaoxue Zhou
Jingyi Wang
Jiancheng Han
Mengmeng Liang
Hongjia Zhang
Yihua He

Frontiers in Genetics

doi 10.3389/fgene.2022.821226

4,018 views
5 citations

Original Research

Published on 24 May 2023

Genetic landscape in Russian patients with familial left ventricular noncompaction

in Cardiovascular Genetics and Systems Medicine

Alexey N. Meshkov
Roman P. Myasnikov
Anna V. Kiseleva
Olga V. Kulikova
Evgeniia A. Sotnikova
Maria M. Kudryavtseva
Anastasia A. Zharikova
Sergey N. Koretskiy
Elena A. Mershina
Vasily E. Ramensky

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1205787

4,689 views
13 citations

Original Research

Accepted on 26 Feb 2026

Clinical Characteristics and Short-Term Outcomes of Left Ventricular Noncompaction Cardiomyopathy in Neonates

in Neonatology

Yan Chen
Yalan Liu
Hua Peng
Yue Song
Ziang Liu

Frontiers in Pediatrics

Case Report

Published on 08 Jun 2023

Low-frequency maternal novel MYH7 mosaicism mutation in recurrent fetal-onset severe left ventricular noncompaction: a case report

in Pediatric Cardiology

Hiroshi Kawamura
Masamichi Ikawa
Keiichi Hirono
Junya Kimura
Takashi Okuno
Masao Kawatani
Kunihiro Inai
Yukiko Hata
Naoki Nishida
Yoshio Yoshida

Frontiers in Pediatrics

doi 10.3389/fped.2023.1195222

3,261 views
1 citation

Case Report

Published on 30 Mar 2021

Case Report: Novel Likely Pathogenic ACTN2 Variant Causing Heterogeneous Phenotype in a Korean Family With Left Ventricular Non-compaction

in Genetics of Common and Rare Diseases

Joonhong Park
Yong Gon Cho
Ha Wook Park
Jung Sun Cho

Frontiers in Pediatrics

doi 10.3389/fped.2021.609389

5,661 views
12 citations

Articles

Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report

Case report: A rare case of left ventricular noncompaction in two Chinese siblings with becker muscular dystrophy caused by deletion of exons 10 to 12 in the DMD gene

Case Report: Biventricular Noncompaction Cardiomyopathy With Pulmonary Stenosis and Bradycardia in a Fetus With KCNH2 Mutation

Genetic landscape in Russian patients with familial left ventricular noncompaction

Clinical Characteristics and Short-Term Outcomes of Left Ventricular Noncompaction Cardiomyopathy in Neonates

Low-frequency maternal novel MYH7 mosaicism mutation in recurrent fetal-onset severe left ventricular noncompaction: a case report

Case Report: Novel Likely Pathogenic ACTN2 Variant Causing Heterogeneous Phenotype in a Korean Family With Left Ventricular Non-compaction