肾源性尿崩症
X染色体
表型
肾
肾脏疾病
医学
肾脏疾病
疾病
内科学
内分泌学
遗传性疾病
阿尔波特综合征
遗传学
生物
肾小球肾炎
基因
作者
Catherine Quinlan,Michelle N. Rheault
标识
DOI:10.1016/j.semnephrol.2022.04.002
摘要
A number of genes that cause inherited kidney disorders reside on the X chromosome. Given that males have only a single active X chromosome, these disorders clinically manifest primarily in men and boys. However, phenotypes in female carriers of X-linked kidney conditions are becoming more and more recognized. This article reviews the biology of X inactivation as well as the kidney phenotype in women and girls with a number of X-linked kidney disorders including Alport syndrome, Fabry disease, nephrogenic diabetes insipidus, X-linked hypophosphatemic rickets, Dent disease, and Lowe syndrome.
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