Suppr超能文献

[伴有转化生长因子-β1 型受体基因突变的非马凡综合征家族性主动脉夹层]

[Familial aortic dissection of non-Marfan syndrome with mutations in the transforming growth factor-beta receptor type 1 genes].

作者信息

Suzuki Ryo, Mikamo Akihito, Kurazumi Hiroshi, Sato Masafumi, Ikeda Yoshitaka, Shirasawa Bungo, Hamano Kimikazu

机构信息

Department of Cardiac Surgery, Yamaguchi University, Ube, Japan.

出版信息

Kyobu Geka. 2011 Feb;64(2):99-104.

Abstract

Marfan syndrome is an inherited connective tissue disorder with ocular, skeletal and cardiovascular systems and often causes acute aortic dissection. Interestingly, there have been several reports of familial thoracic aortic dissection in patients with autosomal dominant diseases without Marfan syndrome. Variation of the transforming growth factor-beta receptor (TGFBR) gene is reported to be one of the causes. We report a case of a familial aortic dissection not associated with Marfan syndrome, with mutation of TGFBR type 1. Hereditary aortic dissection of the non-Marfan syndrome that does not have clinical manifestations is not uncommon. Thus, the existence of familial aortic aneurysm should be in mind in diagnosis and treatment.

摘要

马凡综合征是一种遗传性结缔组织疾病,累及眼、骨骼和心血管系统,常导致急性主动脉夹层。有趣的是,有几篇报道称,患有非马凡综合征的常染色体显性疾病患者出现家族性胸主动脉夹层。据报道,转化生长因子-β受体(TGFBR)基因变异是病因之一。我们报告一例与马凡综合征无关的家族性主动脉夹层病例,该病例存在1型TGFBR突变。无临床表现的非马凡综合征遗传性主动脉夹层并不少见。因此,在诊断和治疗中应考虑家族性主动脉瘤的存在。

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