Clinical manifestations and gene mutation analysis of children with noncompaction of the ventricular myocardium: an analysis of 6 cases.
- Author:
Feng-Hua ZHANG
1
;
Jin-Dou AN
1
;
Song FENG
1
;
Xiao-Jian ZHANG
1
;
Xiao-Lin ZHAO
1
Author Information
1. Department of Pediatrics, First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
- Publication Type:Journal Article
- MeSH:
Cardiomyopathies;
Child;
Child, Preschool;
Echocardiography;
Female;
Heart Ventricles/diagnostic imaging*;
Humans;
Infant;
Male;
Mutation;
Myocardium
- From:
Chinese Journal of Contemporary Pediatrics
2021;23(1):84-90
- CountryChina
- Language:Chinese
-
Abstract:
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 mutations were detected in 4 children, among whom 2 had
