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特发性矮身材病因的研究进展

Research progress of etiology of idiopathic short stature

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【作者】 栗瑶王硕邵娜黄大元谭传梅

【Author】 LI Yao;WANG Shuo;SHAO Na;HUANG Da yuan;TAN Chuan mei;Jishou University School of Medicine;Department of Pediatrics,the First People’s Hospital of Changde City,Hu’nan Province;

【通讯作者】 谭传梅;

【机构】 吉首大学医学院湖南省常德市第一人民医院儿科

【摘要】 特发性矮身材(idiopathic short stature,ISS)是儿童矮身材中最常见的类型,其发病机制尚不明确。尽管ISS可应用生长激素治疗,但是疗效有限,这促使临床医生不断探究ISS的病因。近来研究显示ISS病因与内分泌、信息传递途径的缺陷及其相关基因的突变等因素有关,现总结为以下几点:生长激素-胰岛素样生长因子1(GH-IGF-1)轴及相关基因;软骨生长板的相关基因及激素;其他相关因素。本文就近几年ISS病因研究进展作一综述。

【Abstract】 Idiopathic short stature(ISS) is the most common type in children with short stature, and its pathogenesis is unclear. Although ISS can be treated with growth hormone, its efficacy is limited, which has prompted clinicians to further explore the etiology of ISS. Recent studies have shown that the etiology of ISS is related to endocrine, defect of information transmission pathway and mutation of related genes, which are summarized as follows: growth hormone-insulin-like growth factor 1(GH-IGF-1) axis and related genes, the related genes and hormones of the cartilage growth plate and other relevant factors. This article reviews the etiology of ISS in recent years.

【基金】 湖南省常德市科学技术局技术研究与开发资金项目(2017S032)
  • 【文献出处】 中国当代医药 ,China Modern Medicine , 编辑部邮箱 ,2019年22期
  • 【分类号】R725.8
  • 【被引频次】6
  • 【下载频次】321
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