论文部分内容阅读
对正常人和侏儒症、肢端巨大症等患者进行hGH水平测定及功能试验。结果36例正常人hGH基础值多数小于5μg/L(0.6±0.83),100例正常人活动值多数小于10μg/L(2.36±3.81)。垂体性侏儒症患者hGH一般低于正常,对胰岛素低血糖,多巴胺兴奋试验缺乏正常反应。肢端巨大症患者hGH均高于20μg/L,且不受葡萄糖抑制。提示hGH水平测定及分泌功能试验有助于侏儒症和肢端巨大症的诊断及判断后者活动与否。溴隐亭敏感试验有助于肢端巨大症疗效预测。
In normal and dwarfism, acromegaly patients such as hGH levels and functional tests. Results The majority of 36 normal subjects were less than 5μg / L (0.6 ± 0.83). Most of 100 normal subjects were less than 10μg / L (2.36 ± 3.81). HGH in patients with pituitary dwarfism is generally lower than normal, lack of normal response to insulin hypoglycemia, dopamine excitability test. Patients with acromegaly hGH were higher than 20μg / L, and not inhibited by glucose. Tip hGH level determination and secretion test contribute to the diagnosis of dwarfism and acromegaly and determine the activity of the latter. Bromocriptine sensitivity test contributes to the prediction of acromegaly.