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先天性高胰岛素血症的遗传发病机制及诊疗进展 被引量:13

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摘要 先天性高胰岛素血症(CHI)是婴幼儿和儿童期持续性复发性低血糖的重要原因之一,以胰岛素分泌调节异常,从而造成严重、持续性的低血糖为特征。本病由MacQuarrie于1954年首次描述,诊断为“婴儿特发性低血糖症。”为避免混淆,目前倾向于将生后不久发病的持续性高胰岛素血症称为CHI。近年来,随着分子遗传学的发展和对胰岛细胞生化通路了解的加深,对CHI发病机制的研究及诊断治疗等方面均取得了长足进展,本文就CHI的遗传发病机制及诊疗进展作一综述。
作者 桑艳梅 苞山
出处 《中国糖尿病杂志》 CAS CSCD 北大核心 2009年第9期713-715,共3页 Chinese Journal of Diabetes
基金 北京市科委科技新星培养计划专项基金(9558102700)
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参考文献13

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同被引文献119

  • 1刘振球,余加林.早产儿低血糖研究进展[J].中国循证儿科杂志,2008,3(5):381-386. 被引量:14
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  • 3Jaya Sujatha Gopal-Kothapani,Khalid Hussain.Congenital hyperinsulinism:Role of fluorine-18L-3, 4 hydroxyphenylalanine positron emission tomography scanning[J].World Journal of Radiology,2014,6(6):252-260. 被引量:3
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