Asia Saba, Vaziri Nasab Hamed, Sabbaghian Marjan, Kalantari Hamid, Zari Moradi Shabnam, Gourabi Hamid, Mohseni Meybodi Anahita
Department of Genetics at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Department of Andrology at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Cell J. 2014 Fall;16(3):377-82. Epub 2014 Oct 4.
Complex chromosomal rearrangements (CCRs) are rare events involving more than two chromosomes and over two breakpoints. They are usually associated with infertility or sub fertility in male carriers. Here we report a novel case of a CCR in a 30-year-old oligoasthenosperm man with a history of varicocelectomy, normal testes size and normal endocrinology profile referred for chromosome analysis to the Genetics unit of Royan Reproductive Biomedicine Research Center. Chromosomal analysis was performed using peripheral blood lymphocyte cultures and analyzed by GTG banding. Additional tests such as C-banding and multicolor fluorescence in situ hybridization (FISH) procedure for each of the involved chromosomes were performed to determine the patterns of the segregations. Y chromosome microdeletions in the azoospermia factor (AZF) region were analyzed with multiplex polymerase chain reaction. To identify the history and origin of this CCR, all the family members were analyzed. No micro deletion in Y chromosome was detected. The same de novo reciprocal exchange was also found in his monozygous twin brother. The other siblings and parents were normal. CCRs are associated with male infertility as a result of spermatogenic disruption due to complex meiotic configurations and the production of chromosomally abnormal sperms. These chromosomal rearrangements might have an influence on decreasing the number of sperms.
复杂染色体重排(CCR)是涉及两条以上染色体和两个以上断点的罕见事件。它们通常与男性携带者的不育或生育力低下有关。在此,我们报告了一例30岁少弱精子症男性的CCR新病例,该男性有精索静脉曲张切除术史,睾丸大小正常,内分泌 profile 正常,因染色体分析被转诊至罗扬生殖生物医学研究中心遗传学部门。使用外周血淋巴细胞培养进行染色体分析,并通过GTG显带进行分析。对每条受累染色体进行了额外的检测,如C显带和多色荧光原位杂交(FISH)程序,以确定分离模式。用多重聚合酶链反应分析无精子症因子(AZF)区域的Y染色体微缺失。为了确定该CCR的历史和起源,对所有家庭成员进行了分析。未检测到Y染色体微缺失。在他的同卵双胞胎兄弟中也发现了相同的新发相互交换。其他兄弟姐妹和父母均正常。由于复杂的减数分裂构型导致生精破坏以及产生染色体异常精子,CCR与男性不育有关。这些染色体重排可能会影响精子数量的减少。