无精和严重少精症患者的遗传缺陷分析——附2例世界首报染色体异常核型  

Analysis on Genetic Defects of Patients with Azoospermia and Severe Oligospermia——Report of Two Novel Abnormal Karyotypes

作　　者：张晓云[1] 李永全[1] 郑克勤[1] 周汝滨[1] 陈小萍[1] 廖霞[1] 

机构地区：[1]广东医学院医学遗传学研究室,湛江524023

出　　处：《遗传》2006年第6期646-651,共6页Hereditas（Beijing)

基　　金：广东医学院科研基金资助项目(编号:0412)~~

摘　　要：对217例无精和严重少精症患者外周血淋巴细胞染色体核型进行分析,并采用聚合酶链反应对7例Y染色体结构异常患者的AZFc区进行检测。187例无精症患者中检出异常核型77例(41.18%)(其中46,XY,t(6;14)(p21;p13),46,XY,t(8;12)(p21;q24)为世界首报核型),主要涉及染色体异常(数目异常和结构异常);染色体异态(Y染色体异态和9号染色体臂间倒位)及46,XX性反转;30例严重少精症患者中检出异常核型4例(13.33%)(结构异常和46,XX性反转)。由此可见,性染色体数目和结构异常是精子发生障碍的主要原因,其次常染色体的某些断裂点也可能影响精子发生。AZFc区的缺失与否与精子发生也有直接关系。G banding karyotype analysis of peripheral lymphocytes in 217 patients with azoospermia or severe oligospermia were performed and the Y-chromosome AZFc region from seven cases with Y chromosome abnormality was amplified by polymerase chain reaction （PCR）. Out of 187 cases with azoospermia, 77 patients or 41.18% had chromosome abnormalities, including number and structural aberrations, heteromorphic chromosomes （Y chromosome heteromorphisms and pericentric inversion of chromosome 9） and 46, XX sex reversal. Two novel abnormal karyotypes were found： 46,XY,t（6; 14）（p21 ;p13） and 46,XY,t（8;12）（p21 ;q24）. Out of 30 patients with severe oligospermia, four had chromosome abnormalities, including structural aberration and 46,XX sex reversal. Therefore, aberration of the sex chromosome causes the most serious spermatogenic failure and certain breakpoints in the autosomes may also affect spermatogenesis. The deletion of AZFc also affects spermatogenesis.

关 键 词：无精症 严重少精症 染色体畸变 AZFc区 

分 类 号：R698.2[医药卫生—泌尿科学]