Suppr超能文献

[男性不育的遗传学]

[Genetics of male infertility].

作者信息

Tüttelmann F, Gromoll J, Kliesch S

机构信息

Institut für Humangenetik, Westfälische Wilhelms-Universität, Münster.

出版信息

Urologe A. 2008 Dec;47(12):1561-2, 1564-7. doi: 10.1007/s00120-008-1804-4.

Abstract

Genetic causes of male infertility increase in frequency with decreasing sperm concentration (oligo-/azoospermia). The decision about genetic tests should be made after a complete andrological work-up. Common causes comprise chromosomal aberrations (including Klinefelter syndrome), microdeletions of the AZF loci of the Y chromosome, mutations in the gene responsible for cystic fibrosis (CFTR) causing CBAVD and in genes involved in hypogonadotropic hypogonadism (including Kallmann syndrome). Every genetic investigation should be accompanied by comprehensive genetic counselling to help with the interpretation of results and support the patient/the couple concerning consequences for their family planning and treatment options.

摘要

男性不育的遗传原因随着精子浓度降低(少精子症/无精子症)而愈发常见。在进行全面的男科检查后,再决定是否进行基因检测。常见病因包括染色体畸变(包括克氏综合征)、Y染色体AZF位点微缺失、导致先天性双侧输精管缺如(CBAVD)的囊性纤维化跨膜传导调节因子(CFTR)基因突变以及与低促性腺激素性性腺功能减退相关的基因突变(包括卡尔曼综合征)。每项基因检测都应辅以全面的遗传咨询,以帮助解读检测结果,并在计划生育和治疗方案的后果方面为患者/夫妇提供支持。

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