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Clinical manifestations and gene mutation analysis of children with noncompaction of the ventricular myocardium: an analysis of 6 cases / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics ; (12): 84-90, 2021.
Article in Chinese | WPRIM | ID: wpr-879814
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
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Echocardiography / Heart Ventricles / Mutation / Cardiomyopathies / Myocardium Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: Chinese Journal: Chinese Journal of Contemporary Pediatrics Year: 2021 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Echocardiography / Heart Ventricles / Mutation / Cardiomyopathies / Myocardium Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: Chinese Journal: Chinese Journal of Contemporary Pediatrics Year: 2021 Type: Article