›› 2009, Vol. 29 ›› Issue (11): 1383-.

• Review • Previous Articles     Next Articles

Research on autosomal dominant polycystic kidney disease

YU Guo-peng, reviewer;QI Jun, reviser   

  1. Department of Urologic Surgery, Xinhua Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200092, China
  • Online:2009-11-25 Published:2009-11-24

Abstract:

Polycystic kidney disease is a common human congenital hereditary disease, which can be divided into autosomal dominant polycystic kidney disease and autosomal recessive polycystic kidney disease by genetic methods. In addition to the kidney changes, polycystic kidney disease may also involve multiple body organs and seriously endanger human health. In recent years, studies on etiology and pathogenesis (especially molecular biology), diagnosis and treatment of polycystic kidney disease have progressed by leaps and bounds. This paper briefly summaries the research status and development of the most common autosomal dominant polycystic kidney disease.

Key words: polycystic kidney disease, autosomal dominant, polycystin, gene