...
首页> 外文期刊>Journal of Clinical and Diagnostic Research >A Rare Presentation of theKlinefelter?s Syndrome
【24h】

A Rare Presentation of theKlinefelter?s Syndrome

机译:克莱恩费尔特氏综合症的罕见表现

获取原文
   

获取外文期刊封面封底 >>

       

摘要

A 16 years old boy with Chronic Renal Failure (CRF) was not suspected of having Klinefelter?s syndrome until he complained of painful gynecomastia. He was under haemodialysis for 2 years. At first, he was in an approximately full pubertal development (P5, G5), but he had a small and a firm testis (length 2.2cm) and some degree of facial male pattern hair. He also had a decreased upper to lower body segment ratio and despite having chronic renal failure, he was taller than his parents and siblings. His laboratory tests showed high levels of FSH and normal levels of LH and testosterone. With regards to all these findings, we suspected that there might be an occult Klinefelter?s syndrome. So, we made his karyotype that showed a 47XXY pattern. Because there are only a few number of cases that have occult Klinefelter?s syndrome in the basis of chronic renal failure, we decided to report this case.
机译:一名16岁男孩患有慢性肾功能衰竭(CRF),直到他抱怨有痛苦的女性乳房发育症,才被怀疑患有Klinefelter综合征。他正在接受血液透析2年。刚开始时,他处于青春期左右(P5,G5),但是睾丸小而结实(长2.2cm),并且有一定程度的面部男性花样。他的上半身和下半身比例也有所下降,尽管患有慢性肾功能衰竭,但他比父母和兄弟姐妹高。他的实验室测试显示FSH含量高,LH和睾丸激素含量正常。关于所有这些发现,我们怀疑可能存在隐匿性克氏综合征。因此,我们将其核型显示为47XXY模式。因为只有少数病例因慢性肾功能衰竭而患有隐匿性克氏综合征,所以我们决定报告此病例。

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