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非梗阻性无精子症与父源常染色体环状染色体:病例报告及文献复习。

Azoospermia and paternal autosomal ring chromosomes: case report and literature review.

机构信息

The St. George Hospital, University of New South Wales, Sydney, Australia.

出版信息

Reprod Biomed Online. 2011 Oct;23(4):466-70. doi: 10.1016/j.rbmo.2011.05.013. Epub 2011 May 27.

Abstract

Two men of the same family presented with ring chromosome 22 and azoospermia. The literature on all autosomal ring chromosomes and semen abnormalities was reviewed. Autosomal ring chromosomes were often associated with a low sperm count. This is probably as a result of gamete instability at meiosis due to the ring chromosome which leads to an increased breakdown. In addition, ring chromosomes transmitted from the parents may manifest quite differently in the progeny. Prior to treating these patients with assisted reproduction, appropriate counselling should be offered, in view of the varying phenotypic manifestations of ring chromosomes in the resulting progeny, and prenatal diagnosis or preimplantation diagnosis must be considered.

摘要

两名来自同一家庭的男性均患有环状染色体 22 号和无精子症。我们回顾了所有常染色体环状染色体和精液异常的文献。常染色体环状染色体通常与精子计数低有关。这可能是由于减数分裂过程中环状染色体导致的配子不稳定,从而增加了断裂。此外,来自父母的环状染色体在后代中可能表现出明显不同。鉴于环状染色体在后代中的表型表现各不相同,在对这些患者进行辅助生殖治疗之前,应提供适当的咨询,并考虑进行产前诊断或胚胎植入前诊断。

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