首页> 外文期刊>American journal of medical genetics, Part A >Maternal inheritance of BDNF deletion, with phenotype of obesity and developmental delay in mother and child
【24h】

Maternal inheritance of BDNF deletion, with phenotype of obesity and developmental delay in mother and child

机译:BDNF缺失的母体遗传,母亲和儿童肥胖和发育延迟表型

获取原文
获取原文并翻译 | 示例
           

摘要

Childhood obesity is a significant world health problem. Understanding the genetic and environmental factors contributing to the development of obesity in childhood is important for the rational design of strategies for obesity prevention and treatment. Brain‐derived neurotrophic factor (BDNF) plays an important role in the growth and development of the central nervous system, there is also an evidence that BDNF plays a role in regulation of appetite. Disruption of the expression of this gene in a child has been previously reported to result in a phenotype of severe obesity, hyperphagia, impaired cognitive function, and hyperactivity. We report a mother and child, both with micro‐deletions encompassing the BDNF gene locus, who both have obesity and developmental delay, although without hyperactivity. This report highlights the maternal inheritance of a rare genetic cause of childhood obesity.
机译:儿童肥胖是一个重要的世界健康问题。 了解患有肥胖发展的遗传和环境因素对童年的发展是对肥胖预防和治疗策略的合理设计很重要。 脑衍生的神经营养因子(BDNF)在中枢神经系统的生长和发展中起着重要作用,还有一种证据表明BDNF在对食欲的调节中发挥作用。 先前据报道,在儿童中突破该基因的表达,导致严重肥胖,过度障碍,认知功能和多动症的表型。 我们报告了母亲和孩子,既是含有BDNF基因座的微缺失,既具有肥胖和发育延迟,虽然没有多动症。 本报告突出了儿童肥胖罕见遗传原因的母亲遗传。

著录项

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