Research progress on phenotype and mechanism of cardiac disease caused by CACNA1C gene mutations
10.3760/cma.j.issn.2095-428X.2019.20.017
- VernacularTitle: CACNA1C基因突变致心脏疾病表型及机制的研究进展
- Author:
Zhongman ZHANG
1
;
Yuming QIN
;
Shiwei YANG
Author Information
1. Department of Cardiology, Children′s Hospital of Nanjing Medical University, Nanjing 210009, China
- Publication Type:Review
- Keywords:
CACNA1C gene;
Hereditary arrhythmia;
Cardiomyopathy;
Gene mutation
- From:
Chinese Journal of Applied Clinical Pediatrics
2019;34(20):1587-1590
- CountryChina
- Language:Chinese
-
Abstract:
Mutations in the CACNA1C gene which encodes the α1C subunit of voltage dependent l-type Ca2+ channel can cause mental and cardiovascular diseases.It is the pathogenic gene of Timothy syndrome.Its cardiovascular-system phenotype mainly includes long QT syndrome, Brugada syndrome, short QT syndrome, etc.In recent years, it has been found that CACNA1C gene mutations can also lead to non-syndromic phenotypes, including congenital heart disease, cardiomyopathy, etc, further enriching the clinical phenotype of CACNA1C gene mutation.Now, the recent advances in heart disease phenotypes and mechanisms involved in CACNA1C gene mutations are reviewed.
