Progress of research on the role of CLCNKB gene in classical Bartter syndrome.
10.3760/cma.j.issn.1003-9406.2020.05.020
- Author:
Jiaran ZHOU
1
;
Chunli WANG
;
Huaying BAO
Author Information
1. Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu 210000, China. baohy67@hotmail.com.
- Publication Type:Case Reports
- MeSH:
Asian Continental Ancestry Group;
Bartter Syndrome;
genetics;
pathology;
Chloride Channels;
genetics;
Genetic Association Studies;
Humans;
Research;
trends
- From:
Chinese Journal of Medical Genetics
2020;37(5):573-577
- CountryChina
- Language:Chinese
-
Abstract:
Bartter syndrome is an inherited metabolic disorder characterized by hypokalemic alkalosis and high rennin-angiotensin-aldosteronism which can occur at all ages but mainly in childhood. Classical Bartter syndrome is caused by loss-of-function variants in the gene encoding basolateral chloride channel ClC-Kb (CLCNKB), which is a common type of Bartter syndrome characterized with diverse clinical manifestations ranging from severe to very mild. This article reviews the function and mechanism of CLCNKB variants in Chinese population and the genotype-phenotype correlation of CLCNKB variants in classical Bartter syndrome.
