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The correlation of leptin/leptin receptor gene polymorphism and insulin-like growth factor-1 and their impact on childhood growth hormone deficiency

机译:瘦素/瘦素受体基因多态性与胰岛素样生长因子-1的相关性及其对儿童生长激素缺乏的影响

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OBJECTIVE: Growth hormone deficiency (GHD) is the most common cause for childhood dwarfism. Currently, the significance of insulin-like growth factor-1 (IGF-1) in diagnosis of GHD is still debatable. Due to the possible correlation between leptin (LEP) and GHD pathogenesis, this study investigated the gene polymorphism of LEP and its receptor (LEPR) genes, along with serum IGF-1 and LEP levels in GHD patients. This study attempted to illustrate the correlation between gene polymorphism and GHD pathogenesis.
机译:目的:生长激素缺乏症(GHD)是儿童侏儒症最常见的原因。目前,胰岛素样生长因子-1(IGF-1)在GHD诊断中的意义尚有争议。由于瘦素(LEP)与GHD发病机制之间可能存在相关性,本研究调查了GHD患者LEP及其受体(LEPR)基因的多态性,以及血清IGF-1和LEP水平。这项研究试图说明基因多态性与GHD发病机制之间的相关性。

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