疾病
常染色体显性多囊肾病
多囊肾病
遗传异质性
医学
包装D1
生物信息学
肾脏疾病
遗传性疾病
生物
遗传学
基因
病理
内科学
表型
作者
Vicente E. Torres,Peter C. Harris,Yves Pirson
出处
期刊:The Lancet
[Elsevier BV]
日期:2007-04-01
卷期号:369 (9569): 1287-1301
被引量:1467
标识
DOI:10.1016/s0140-6736(07)60601-1
摘要
Autosomal dominant polycystic kidney disease is the most prevalent, potentially lethal, monogenic disorder. It is associated with large interfamilial and intrafamilial variability, which can be explained to a large extent by its genetic heterogeneity and modifier genes. An increased understanding of the disorder's 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 treatments.
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