Genetic and spermatological aspects of acephalic sperm syndrome

S. S. Khayat, E. Bragina, L. Kurilo, V. Chernykh
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Abstract

Acephalic sperm syndrome is a genetically determined form of primary male infertility associated with teratozoospermia due to  a  disrupted  head-tail  coupling  apparatus.  Acephalic  spermatozoa  syndrome  is  characterized  by  high  proportion of headless (acephalic) spermatozoa in the ejaculate. Sperm morphological changes in this syndrome were characterized, however, the etiology and pathogenesis of this syndrome have not been under evaluated. In recent years, with the progress in sequencing technology and other high-performance methods of genome, proteome and other omics technologies, it has become possible to identify many genetic causes of disorders of spermatogenesis and male infertility, as well as a better understanding of their mechanisms. This article provides a brief overview of the genes associated with acephalic sperm syndrome.
畸形精子症的遗传学和精子学问题
畸形精子症是一种由基因决定的原发性男性不育症,由于头尾耦合装置紊乱而导致畸形精子症。 畸形精子综合征的特点是射出的精子中无头(畸形)精子比例高。该综合征的精子形态变化已被定性,但其病因和发病机制尚未得到充分评估。近年来,随着基因组、蛋白质组和其他omics技术的测序技术和其他高性能方法的进步,已经可以确定精子发生障碍和男性不育症的许多遗传原因,并对其机制有了更好的了解。本文简要概述了与 "畸形精子症 "相关的基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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