首页> 外文期刊>Balkan journal of medical genetics: BJMG >HYPERGONADOTROPIC HYPOGONADISM, PROGRESSIVE EARLY-ONSET SPINOCEREBELLAR ATAXIA, AND LATE-ONSET SENSORINEURAL HEARING LOSS: CASE REPORT AND LITERATURE REVIEW
【24h】

HYPERGONADOTROPIC HYPOGONADISM, PROGRESSIVE EARLY-ONSET SPINOCEREBELLAR ATAXIA, AND LATE-ONSET SENSORINEURAL HEARING LOSS: CASE REPORT AND LITERATURE REVIEW

机译:雌性性腺功能减退症,进展性早发性脊椎小囊性轴索病和迟发性感觉神经性听力损失:病例报告和文献复习

获取原文
获取原文并翻译 | 示例
           

摘要

The association of ataxia, hypergonadotropic hy-pogonadism and hearing loss is extremely rare. Considerable heterogeneity exists in the literature of the neurological manifestations, age of onset, clinical severity and associated abnormalities. We describe a 24-year-old woman with secondary hypergonadotropic amenorrhea, early-onset progressive spinocerebellar ataxia (SCA), late-onset sensorineural hearing loss and normal intelligence and compare it with reported cases.
机译:共济失调,促性腺激素低下性腺功能减退症和听力下降的关联极为罕见。在神经系统表现,发病年龄,临床严重程度及相关异常的文献中存在相当多的异质性。我们描述了一名患有继发性促性腺激素性闭经,早发性进行性脊髓小脑性共济失调(SCA),迟发性感音神经性听力下降和智力正常的24岁女性,并将其与报道的病例进行比较。

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