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膀胱外翻-尿道上裂复合畸形

Bladder exstrophy-epispadias complex.

作者信息

Ludwig Michael, Ching Bonnie, Reutter Heiko, Boyadjiev Simeon A

机构信息

Department of Clinical Chemistry and Pharmacology, University of Bonn, Sigmund-Freud-Str. 25, Bonn D-53105, Germany.

出版信息

Birth Defects Res A Clin Mol Teratol. 2009 Jun;85(6):509-22. doi: 10.1002/bdra.20557.

Abstract

The bladder exstrophy-epispadias complex (BEEC) represents an anterior midline defect with variable expression comprising a spectrum of anomalies involving the abdominal wall, pelvis, urinary tract, genitalia, and occasionally the spine and anus. The vast majority of BEEC cases are classified as non-syndromic and the etiology of this malformation is still unknown. This review presents the current state of knowledge on this multifactorial disorder, including historical retrospect, phenotypic and anatomical characterization, epidemiology, proposed developmental mechanisms, existing animal models, and implicated genetic and environmental components. These published lines of evidence argue strongly that BEEC occurs as a result of strong genetic predisposition that is yet to be deciphered.

摘要

膀胱外翻-尿道上裂复合体(BEEC)是一种前中线缺损,表现多样,包括一系列涉及腹壁、骨盆、泌尿道、生殖器的异常,偶尔还涉及脊柱和肛门。绝大多数BEEC病例被归类为非综合征性,这种畸形的病因仍不清楚。本综述介绍了关于这种多因素疾病的当前知识状态,包括历史回顾、表型和解剖特征、流行病学、提出的发育机制、现有的动物模型以及相关的遗传和环境因素。这些已发表的证据有力地表明,BEEC是由尚未被破解的强烈遗传易感性导致的。

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