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精子发生障碍的遗传学研究进展

曹云霞 高明

国际生殖健康/计划生育杂志Issue(3):182-185,4.
国际生殖健康/计划生育杂志Issue(3):182-185,4.

精子发生障碍的遗传学研究进展

Genetic Research on Male Spermatogenic Failure

曹云霞 1高明1

作者信息

  • 1. 230022合肥,安徽医科大学第一附属医院生殖医学中心
  • 折叠

摘要

Abstract

Approximately 10%-15% of couples are infertile, while male infertility is almost half of all infertility. Spermatogenic failure is a major cause of male infertility, which shows azoospermia or oligozoospermia. Studies showed that Y chromosome plays an important role in spermatogenesis, and that Yq microdeletions are related to male infertility. X chromosome, as a single copy and unique expression in male, also plays an important role in spermatogenesis. Studies on teratozoospermia and asthenozoospermia showed that four genes located on autosomal chromosomes(SPATA16, PICK1,CATSPER and AURKC) probably involved in spermatogenic failure. In future, more and more new genetic tests will be developed and used in the clinical practice of spermatogenic failure, with the worldwide efforts.

关键词

不育,男(雄)性/遗传学,医学/基因/精子发生/无精子症/少精子症/弱精子症

Key words

Infertility,male/Genetics,medical/Genes/Spermatogenesis/Azoospermia/Oligospermia/Astheno-zoospermia

引用本文复制引用

曹云霞,高明..精子发生障碍的遗传学研究进展[J].国际生殖健康/计划生育杂志,2014,(3):182-185,4.

国际生殖健康/计划生育杂志

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