Suppr超能文献

卡尔曼综合征患者的临床特征和睾丸形态。

Clinical features and testicular morphology in patients with Kallmann syndrome.

机构信息

Department of Nephro-urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan.

出版信息

Urology. 2012 Mar;79(3):684-6. doi: 10.1016/j.urology.2011.10.032. Epub 2011 Dec 14.

Abstract

Kallmann syndrome (KS) is a genetic disorder characterized by the simultaneous occurrence of idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. Here, we present 3 cases of KS with detailed description. In Case 1, testicular morphology was examined by testicular biopsy, and Leydig cells were examined by immunohistochemistry using antibodies against Ad4BP/SF1. Contrary to our predictions, the present study revealed the presence of Leydig cells in the testis. Testicular morphology in the patients with KS is more varied than expected, and further investigation is required to elucidate hormonal effects on normal testicular development.

摘要

卡尔曼综合征(KS)是一种遗传性疾病,其特征是同时发生特发性促性腺激素低下性性腺功能减退症(IHH)和嗅觉缺失。在这里,我们详细描述了 3 例 KS 病例。在病例 1 中,通过睾丸活检检查睾丸形态,并用针对 Ad4BP/SF1 的抗体通过免疫组织化学检查间质细胞。与我们的预测相反,本研究显示睾丸中存在间质细胞。KS 患者的睾丸形态比预期的更为多样化,需要进一步研究阐明激素对正常睾丸发育的影响。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验