Abyholm T, Stray-Pedersen S
Int J Androl. 1981 Oct;4(5):546-58. doi: 10.1111/j.1365-2605.1981.tb00737.x.
Clinical examinations including cytogenetical analyses were performed in 356 male partners of barren couples, 176 with azoospermia and 180 men with sperm counts below 10 million/ml. The chromosomal aberrations observed were: Klinefelter's syndrome (15 cases), 46 XX (3), 47 XYY (1), Y-chromosome anomalies (5), robertsonian (8) and reciprocal autosomal translocations (1), and 46 XY 16 h + (1). If minor variants were excluded this gave an incidence of constitutional chromosomal abnormalities of 11.9% in the azoospermia group and 4.4% in the oligozoospermia group. The phenotypes expressed by the specific anomalies showed great variations and appeared to be practically indistinguishable from those individuals having a normal karyotype.
对356名不育夫妇的男性伴侣进行了包括细胞遗传学分析在内的临床检查,其中176人无精子症,180人的精子计数低于1000万/毫升。观察到的染色体畸变有:克兰费尔特综合征(15例)、46,XX(3例)、47,XYY(1例)、Y染色体异常(5例)、罗伯逊易位(8例)和常染色体相互易位(1例),以及46,XY 16qh+(1例)。如果排除微小变异,无精子症组的染色体结构异常发生率为11.9%,少精子症组为4.4%。特定异常所表现出的表型差异很大,实际上与核型正常的个体难以区分。