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巴德-比德尔综合征:超越纤毛

Bardet-Biedl syndrome: beyond the cilium.

作者信息

Tobin Jonathan L, Beales Philip L

机构信息

Molecular Medicine Unit, UCL Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.

出版信息

Pediatr Nephrol. 2007 Jul;22(7):926-36. doi: 10.1007/s00467-007-0435-0. Epub 2007 Mar 15.

Abstract

The Bardet-Biedl syndrome (BBS) is a significant genetic cause of chronic and end-stage renal failure in children. Despite being a relatively rare recessive condition, BBS has come to prominence during the past few years owing to revelations of primary cilia dysfunction underlying pathogenesis. The study of this multi-system disorder, which includes obesity, cognitive impairment, genito-urinary tract malformations and limb deformities, is beginning to reveal insights into several aspects of mammalian development and organogenesis. Involvement of BBS proteins in disparate pathways such as the non-canonical Wnt and Sonic Hedgehog pathways is highlighting their interplay in disease pathogenesis. Here we review the recent developments in this emerging field, with the emphasis on the renal component of the syndrome and potential future directions.

摘要

巴德-比德尔综合征(BBS)是儿童慢性和终末期肾衰竭的一个重要遗传病因。尽管BBS是一种相对罕见的隐性疾病,但由于其发病机制中潜在的原发性纤毛功能障碍被揭示,在过去几年中受到了关注。对这种多系统疾病的研究,包括肥胖、认知障碍、泌尿生殖系统畸形和肢体畸形,开始揭示哺乳动物发育和器官发生的几个方面。BBS蛋白参与非经典Wnt和音猬因子等不同途径,这凸显了它们在疾病发病机制中的相互作用。在此,我们综述了这一新兴领域的最新进展,重点关注该综合征的肾脏组成部分以及潜在的未来研究方向。

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