Suppr超能文献

特定先天性畸形中的心脏。关于发病机制关系的一课。

The heart in selected congenital malformations. A lesson in pathogenetic relationships.

作者信息

Thomas I T, Frias J L

出版信息

Ann Clin Lab Sci. 1987 Jul-Aug;17(4):207-10.

PMID:3619396
Abstract

The application of new knowledge on the pathogenesis of congenital heart defects has increased our understanding of associated, non-cardiac malformations seen in certain syndromes. Defects in the proliferation and migration of neural crest cells are thought to contribute to conotruncal defects. These are seen in association with conditions such as DiGeorge syndrome. CHARGE association, hemifacial microsomia, and Shprintzen syndrome. They also form part of the isotretinoin and thalidomide embryopathies. Their association with conotruncal defects suggests that abnormal migration of neural crest cells may play a role in the pathogenesis of these syndromes.

摘要

先天性心脏缺陷发病机制新知识的应用,加深了我们对某些综合征中所见相关非心脏畸形的理解。神经嵴细胞增殖和迁移缺陷被认为与圆锥干缺陷有关。这些缺陷见于诸如迪格奥尔格综合征、CHARGE综合征、半侧颜面短小畸形和施普林曾综合征等疾病。它们也是异维甲酸和沙利度胺胚胎病的一部分。它们与圆锥干缺陷的关联表明,神经嵴细胞的异常迁移可能在这些综合征的发病机制中起作用。

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