首页> 外文期刊>Internal medicine. >Three Japanese patients from two families with generalized resistance to thyroid hormone with mutations in exon 9 of the thyroid hormone receptor beta gene.
【24h】

Three Japanese patients from two families with generalized resistance to thyroid hormone with mutations in exon 9 of the thyroid hormone receptor beta gene.

机译:来自两个家庭的三名日本患者对甲状腺激素具有普遍抵抗性,且甲状腺激素受体β基因的第9外显子发生突变。

获取原文
获取原文并翻译 | 示例
           

摘要

Resistance to thyroid hormone (RTH) is a genetic disorder caused by mutations in the thyroid hormone receptor (TR) beta gene. The mutations are clustered in two regions: exon 9 and exon 10. To date, only one patient with an exon 9 mutation has been reported in Japan. We herein report three patients from two Japanese families with RTH and mutations in exon 9. A 52-year-old woman and her 18-year-old daughter, both with inappropriate secretion of TSH (SITSH) were diagnosed simultaneously with generalized RTH. Molecular analysis revealed a G345D mutation. An 11-year-old girl with SITSH, whose only manifestation was a goiter, had an R338W mutation, which is frequently associated with pituitary RTH. Thus, RTH with mutations in exon 9 of the TR beta gene is not so rare in Japan.
机译:对甲状腺激素(RTH)的抗性是由甲状腺激素受体(TR)β基因突变引起的遗传性疾病。突变集中在两个区域:第9外显子和第10外显子。迄今为止,在日本仅报道了一名外显子9突变的患者。我们在此报告了来自日本两个家庭的三名RTH和外显子9突变的患者。一名52岁的女性和她的18岁的女儿均被诊断为TSH(SITSH)分泌异常,并同时患有全身性RTH。分子分析显示G345D突变。一名11岁的SITSH女孩,唯一的症状是甲状腺肿,具有R338W突变,该突变通常与垂体RTH相关。因此,在日本,TRβ基因外显子9突变的RTH并不罕见。

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