...
【24h】

A proposed classification system for familial intestinal atresia and its relevance to the understanding of the etiology of jejunoileal atresia.

机译:拟议的家族性肠闭锁分类系统及其与对空肠油闭锁病因的理解有关。

获取原文
获取原文并翻译 | 示例
           

摘要

Familial cases of the various types of intestinal atresia are well described, and we now report an additional family. Based on a review of the literature, a classification system for the different types of familial atresia is presented. Current teaching attributes most jejunoileal atresias to in utero vascular accidents occurring relatively late in gestation (after the 11th or 12th week). Although some cases clearly occur this way, as a result of processes such as volvulus and intussusception, knowledge of the familial form of the disease indicates that most cases of jejunoileal atresia actually result from disruption of a normal embryologic pathway, most likely the development of the superior mesenteric artery and its branches. They should be considered to be true embryologic malformations rather than acquired lesions.
机译:各种类型的肠道闭锁的家族病例都得到了很好的描述,我们现在报告一个新的家庭。基于对文献的回顾,提出了针对不同类型的家族性闭锁的分类系统。当前的教学将大多数空肠闭锁归因于在妊娠后期(第11周或第12周之后)发生的子宫内血管意外。尽管某些情况显然是以这种方式发生的,但由于肠扭转和肠套叠等过程,对这种疾病的家族形式的了解表明,空肠空肠闭锁的大多数病例实际上是由于正常胚胎学途径的破坏所致,很可能是空肠发育的结果。肠系膜上动脉及其分支。应该将它们视为真正的胚胎畸形,而不是获得性病变。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号