Tüttelmann F, Gromoll J, Kliesch S
Institut für Humangenetik, Westfälische Wilhelms-Universität, Münster.
Urologe A. 2008 Dec;47(12):1561-2, 1564-7. doi: 10.1007/s00120-008-1804-4.
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.
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。