Recent advances in studies on autosomal dominant adult polycystic kidney disease.
10.3760/cma.j.issn.1003-9406.2010.04.009
- Author:
Chao-wen YU
1
;
Si-zhong ZHANG
Author Information
1. Department of Medical Genetics, West China Medical School, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041 PR China.
- Publication Type:Journal Article
- MeSH:
Aged;
Female;
Humans;
Male;
Middle Aged;
Polycystic Kidney, Autosomal Dominant;
genetics;
Research;
TRPP Cation Channels;
genetics
- From:
Chinese Journal of Medical Genetics
2010;27(4):402-405
- CountryChina
- Language:Chinese
-
Abstract:
Adult polycystic kidney disease (APKD) is a severe autosomal dominant inheritable renal disease with high incidence. Because of the late-onset of the disease, patients might have transferred the disease gene to the next generation when diagnosis is made. Since its pathogenic molecular mechanism is still not completely clear and the shortage of effective medicines, the prevention and treatment of the disease is still not satisfactory. In the present article, the recent advances in the research on the pathogenesis, gene diagnosis and management of APKD are reviewed.
