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特纳综合征患者的生长激素储备能力。

Growth hormone reserve capacity in Turner's syndrome.

作者信息

Laczi F, Julesz J, Janáky T, László F A

出版信息

Horm Metab Res. 1979 Dec;11(12):664-6. doi: 10.1055/s-0028-1092795.

Abstract

In 11 untreated and 6 oestrogen-treated Turner's syndrome patients, the changes in the serum growth hormone level were studied following the induction of hypoglycaemia with insulin. The growth hormone was measured with a radioimmune assay technique. The growth hormone peak value measured in healthy females was 54.32 +/- 17.17, in untreated Turner's syndrome was 14.90 +/- 3.71, and in oestrogen-treated Turner patients was 33.38 +/- 9.22 microU/ml (average +/- standard error). On the basis of the results, a role is attributed to the decreased growth hormone reserve in the low growth of Tuner's syndrome patients.

摘要

在11名未经治疗和6名接受雌激素治疗的特纳综合征患者中,研究了胰岛素诱发低血糖后血清生长激素水平的变化。采用放射免疫分析技术测定生长激素。健康女性的生长激素峰值为54.32±17.17,未经治疗的特纳综合征患者为14.90±3.71,接受雌激素治疗的特纳综合征患者为33.38±9.22微单位/毫升(平均值±标准误差)。根据这些结果,生长激素储备减少被认为在特纳综合征患者生长缓慢中起作用。

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