Suppr超能文献

肾脏和尿路先天性异常(CAKUT)的个体发生

Ontogeny of congenital anomalies of the kidney and urinary tract, CAKUT.

作者信息

Miyazaki Yoichi, Ichikawa Iekuni

机构信息

Departments of Pediatrics and Medicine, Vanderbilt University Medical Center Nashville, TN, USA.

出版信息

Pediatr Int. 2003 Oct;45(5):598-604. doi: 10.1046/j.1442-200x.2003.01777.x.

Abstract

Ectopic budding of the initial ureter from the Wolffian duct is the first ontogenic misstep that leads to many congenital anomalies of the kidney and urinary tract (CAKUT). The ectopia results in hypoplastic kidney, ectopia of ureterovesical orifice, urinary outflow obstruction and/or reflux. Recent studies on several mutant mouse models verified that ectopic ureteric budding indeed occurs prior to the formation of CAKUT. Often, the genes involved in navigating the site of ureteric budding also regulate later ontogenic processes of the kidney and other urinary tract systems. These additional functions of the genes underlie the wide spectrum of CAKUT, for example multicystic dysplastic kidney, megaureter and atretic ureter, because the genes regulate the morphogenesis of the many portions of the excretory system through their distinctive cellular functions.

摘要

输尿管最初从 Wolffian 管异位出芽是导致许多肾脏和尿路先天性异常(CAKUT)的第一个个体发生错误步骤。这种异位会导致肾发育不全、输尿管膀胱开口异位、尿路梗阻和/或反流。最近对几种突变小鼠模型的研究证实,在 CAKUT 形成之前确实会发生输尿管异位出芽。通常,参与引导输尿管出芽部位的基因也调节肾脏和其他尿路系统的后期个体发生过程。这些基因的额外功能是 CAKUT 广泛谱系的基础,例如多囊性发育不良肾、巨输尿管和闭锁性输尿管,因为这些基因通过其独特的细胞功能调节排泄系统许多部分的形态发生。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验