包装D1
等位基因
疾病
遗传学
常染色体显性多囊肾病
多囊肾
生物
多囊肾病
医学
肾
内科学
基因
作者
Ashima Gulati,Neera K. Dahl,Erum A. Hartung,Stephanie Clark,Asha Moudgil,Julie E. Goodwin,Stefan Somlo
出处
期刊:Kidney360
[American Society of Nephrology (ASN)]
日期:2023-03-01
卷期号:4 (3): 387-392
被引量:1
标识
DOI:10.34067/kid.0000000000000064
摘要
Key Points Autosomal dominant polycystic kidney disease (ADPKD) manifesting earlier than expected on the basis of family history can identify clinically tolerant PKD1 alleles with reduced expression. Hypomorphic PKD1 alleles can cause mild kidney disease or liver cysts in the absence of clinically manifest kidney involvement. The presented data highlight pleiotropic ADPKD clinical presentations and varying severity of kidney disease from PKD1 allele combinations.
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