Vidal F, Templado C, Navarro J, Brusadin S, Marina S, Egozcue J
Hum Genet. 1982;60(4):301-4. doi: 10.1007/BF00569207.
We describe the results of meiotic and synaptonemal complex (SC) studies in a selected series of 45 subfertile males with different meiotic and seminal alterations. SC anomalies (pairing anomalies, fragmented SCs, or presynaptic arrest) were observed in 32 cases (71.1%). In 31% of the abnormal cases, meiotic anomalies could only be detected through the study of SCs. The origin of synaptic anomalies may be related to the assembly of myosin molecules along the chromosomes. SC analysis should become routine in the study of subfertile males.
我们描述了对45名患有不同减数分裂和精液异常的亚生育男性进行的减数分裂和联会复合体(SC)研究结果。在32例(71.1%)中观察到SC异常(配对异常、SC片段化或突触前停滞)。在31%的异常病例中,减数分裂异常只能通过SC研究检测到。突触异常的起源可能与肌球蛋白分子沿染色体的组装有关。SC分析应成为亚生育男性研究中的常规操作。