Suppr超能文献

埃布斯坦畸形的一种“先天性矫正型”变异。

A "congenitally corrected" variant of Ebstein's anomaly.

作者信息

Çetin Güvenç Rengin, Akgün Gökmen, Güvenç Tolga S

机构信息

1Department of Cardiology,Dr. Siyami Ersek Cardiovascular and Thoracic Surgery Research and Training Hospital,Istanbul,Turkey.

2Department of Pediatric Cardiology,Dr. Siyami Ersek Cardiovascular and Thoracic Surgery Research and Training Hospital,Istanbul,Turkey.

出版信息

Cardiol Young. 2018 Apr;28(4):608-610. doi: 10.1017/S1047951117002712. Epub 2018 Jan 10.

Abstract

Ebstein's anomaly is a rare CHD that is characterised by caudal displacement of the functional tricuspid annulus and a dysfunctional tricuspid valve owing to a failure of proper leaflet coaptation. We present a balanced variant of Ebstein's anomaly, in which the overgrowth of the septal leaflet had allowed proper coaptation of the tricuspid leaflets, thus preserving the valve function.

摘要

埃布斯坦畸形是一种罕见的先天性心脏病,其特征是功能性三尖瓣环尾端移位以及由于瓣叶不能正常对合导致三尖瓣功能障碍。我们展示了埃布斯坦畸形的一种平衡变异型,其中隔叶过度生长使得三尖瓣叶能够正常对合,从而保留了瓣膜功能。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验