Autosomal dominant polycystic kidney disease: the last 3 years

被引:420
作者
Torres, Vicente E. [1 ]
Harris, Peter C. [1 ]
机构
[1] Mayo Clin, Dept Internal Med, Div Nephrol & Hypertens, Rochester, MN 55905 USA
关键词
ADPKD; PKD1; PKD2; polycystic kidney disease; polycystin-1; polycystin-2; RENAL EPITHELIAL-CELLS; CONVERTING ENZYME-INHIBITION; HAN-SPRD RATS; CYST FORMATION; ENDOPLASMIC-RETICULUM; LIVER CYST; ENDOTHELIAL DYSFUNCTION; PROMOTER POLYMORPHISM; MOLECULAR DIAGNOSTICS; HEPATIC CYSTOGENESIS;
D O I
10.1038/ki.2009.128
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Autosomal dominant polycystic kidney disease is the most prevalent, potentially lethal monogenic disorder. It has large inter-and intra-familial variability explained to a large extent by its genetic heterogeneity and modifier genes. An increased understanding of its underlying genetic, molecular, and cellular mechanisms and a better appreciation of its progression and systemic manifestations have laid out the foundation for the development of clinical trials and potentially effective therapies. The purpose of this review is to update the core of knowledge in this area with recent publications that have appeared during 2006-2009. Kidney International (2009) 76, 149-168; doi: 10.1038/ki.2009.128; published online 20 May 2009
引用
收藏
页码:149 / 168
页数:20
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