Suppr超能文献

一名患有克鲁宗综合征且成纤维细胞生长因子受体(FGFR)-2基因发生突变的患者出现心内膜垫缺损。

Endocardial cushion defect in a patient with Crouzon syndrome carrying a mutation in the fibroblast growth factor receptor (FGFR)-2 gene.

作者信息

Schulz C, Kress W, Schömig A, Wessely R

机构信息

German Heart Center and 1st Department of Medicine, Klinikum rechts der Isar, University of Technology, Lazarettstrasse 36, 80636 Munich, Germany.

出版信息

Clin Genet. 2007 Oct;72(4):305-7. doi: 10.1111/j.1399-0004.2007.00861.x.

Abstract

Crouzon syndrome is an autosomal dominant disorder caused by mutation in the fibroblast growth factor receptor (FGFR)-2 gene. Recent findings from animal studies imply a critical role for FGFs in the regulation of cardiac development including cardiac cushion proliferation and valvulogenesis. We report on a 36-year-old woman, who required surgical closure for an atrial septal defect, a clinical feature that has not been previously reported in other patients with Crouzon syndrome. The findings suggest that cardiac investigations are warranted in patients with a diagnosis of Crouzon syndrome.

摘要

克鲁宗综合征是一种由成纤维细胞生长因子受体(FGFR)-2基因突变引起的常染色体显性疾病。动物研究的最新发现表明,成纤维细胞生长因子(FGFs)在心脏发育调控中起关键作用,包括心脏心垫增殖和瓣膜形成。我们报告了一名36岁女性,她因房间隔缺损需要手术闭合,这是克鲁宗综合征其他患者之前未报道过的临床特征。这些发现表明,对诊断为克鲁宗综合征的患者进行心脏检查是必要的。

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