• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

Concordance of congenital heart defects in two pairs of monozygotic twins: pulmonary stenosis and tetralogy of Fallot.

作者信息

Alva Carlos, Gómez Felipe David, Jimenez-Arteaga Santiago, Yáñez Lucelli, Ochoa Lilia

机构信息

Director of Congenital Heart Disease Department, Hospital, Centro Médico Nacional Siglo XXI.

出版信息

Arch Cardiol Mex. 2010 Jan-Mar;80(1):29-32.

PMID:21147560
Abstract

Two pairs of twins with specific concordance in congenital heart lesions are presented. We reviewed all the monozygotic twins with specific concordance in congenital heart lesions in the last 18 years. Two pairs were found. First, a pair of 13 years-old monozygotic female twins; a severe infundibular and pulmonary valve stenosis was discovered in both girls. In the second pair of twins (8 years-old boys), Tetralogy of Fallot was diagnosed by echocardiogram, cardiac catheterization and angicardiography. In fluorescence hybridization test in situ all patients were negative for microdeletion in chromosome 22q11. Anatomic differences between twins are not enough explained on genetic bases; it's necessary to consider the role of other factors, probably acquired during the first stages of embryonic development. These are the two first pairs of twins with specific concordance in congenital cardiac lesions reported in Mexico.

摘要

相似文献

1
Concordance of congenital heart defects in two pairs of monozygotic twins: pulmonary stenosis and tetralogy of Fallot.
Arch Cardiol Mex. 2010 Jan-Mar;80(1):29-32.
2
Monozygotic twins with chromosome 22q11 microdeletion and discordant phenotypes in cardiovascular patterning.具有22q11染色体微缺失且心血管发育模式表型不一致的同卵双胞胎。
Pediatr Cardiol. 2001 May-Jun;22(3):260-3. doi: 10.1007/s002460010219.
3
Tetralogy of Fallot in monozygotic twins.
Indian Heart J. 2002 Jan-Feb;54(1):83-5.
4
Could submicroscopical chromosomal imbalances cause cono-truncal malformations in twins?亚微观染色体失衡会导致双胞胎的圆锥动脉干畸形吗?
Congenit Heart Dis. 2012 Mar-Apr;7(2):170-7. doi: 10.1111/j.1747-0803.2011.00544.x. Epub 2011 Jul 1.
5
Phenotypic discordance in monozygotic twins with 22q11.2 deletion.患有22q11.2缺失的单卵双胞胎的表型不一致。
Am J Med Genet. 1998 Jul 24;78(4):319-21.
6
[Twins and congenital heart defects].
Helv Paediatr Acta. 1972 Nov;27(5):519-23.
7
[Genetic studies in different types of congenital heart defects].
Monatsschr Kinderheilkd (1902). 1971 Jul;119(7):417-21.
8
[Tetralogy of Fallot in monozygotic twins].
Arch Pediatr. 2001 Apr;8(4):385-8. doi: 10.1016/s0929-693x(00)00215-3.
9
Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.法洛四联症合并肺动脉闭锁伴22q11染色体缺失
J Am Coll Cardiol. 1996 Jan;27(1):198-202. doi: 10.1016/0735-1097(95)00415-7.
10
Persistent truncus arteriosus in monozygotic twins: case report and literature review.单卵双胎中的永存动脉干:病例报告及文献复习
Am J Med Genet. 1999 Jan 15;82(2):146-8. doi: 10.1002/(sici)1096-8628(19990115)82:2<146::aid-ajmg9>3.0.co;2-p.