Salahshourifar I, Shahrokhshahi N, Tavakolzadeh T, Beheshti Z, Gourabi H
Reproductive Genetics Department, Reproductive Medicine Research Center, Royan Institute, ACECR, Tehran, Iran.
J Appl Genet. 2009;50(1):69-72. doi: 10.1007/BF03195655.
Here we describe a rare case of an apparently balanced karyotype of 46, XY, t(1;22;4)(p22.3;q11.1;q31.1) in a infertile male with oligoastenoteratozoospermia (OAT). He was the second patient with complex chromosomal rearrangement (CCR) referred to our center because of infertility. We also review reports on 24 males carrying CCRs with spermatogenesis failure or a malformed child, to provide information on the reproductive outcome of male CCR carriers.
在此,我们描述了一例罕见病例,一名患有少弱畸精子症(OAT)的不育男性,其核型为46, XY, t(1;22;4)(p22.3;q11.1;q31.1),看似平衡。他是因不育转诊至我们中心的第二例患有复杂染色体重排(CCR)的患者。我们还回顾了24例携带CCR且存在精子发生失败或子代畸形的男性的报告,以提供有关男性CCR携带者生殖结局的信息。