首页> 外文期刊>Clinical Pediatric Endocrinology >A Case Report of Turner Syndrome with Graves' Disease during Recombinant Human GH Therapy and Review of Literature
【24h】

A Case Report of Turner Syndrome with Graves' Disease during Recombinant Human GH Therapy and Review of Literature

机译:重组人GH治疗特纳综合症合并格雷夫斯病1例并文献复习

获取原文
           

摘要

An increased incidence of Hashimoto thyroiditis has been reported in patients with Turner syndrome, but several cases of Graves' disease were also described ten to 20 years ago. We report the case of a patient with Turner syndrome who developed Graves' disease, 3 years after successful treatment with recombinant human growth hormone (GH). A diagnosis of Graves' disease was made and treatment with thiamazole was started, which resulted in normalization of the thyroid function. It is important to monitor thyroid function as well as growth parameters in patients with Turner syndrome.
机译:据报道,Turner综合征患者桥本甲状腺炎的发病率增加,但在10至20年前也有几例Graves病病例。我们报告了在成功使用重组人类生长激素(GH)治疗3年后发展为Graves病的特纳综合征患者的病例。诊断为格雷夫斯病并开始用噻唑治疗,从而使甲状腺功能正常化。监测特纳综合征患者的甲状腺功能以及生长参数非常重要。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号