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一名精液参数看似正常的男性出现常染色体易位,作为习惯性流产的一个原因。

Autosomal translocation in an apparently normospermic male as a cause of habitual abortion.

作者信息

Granat M, Aloni T, Makler A, Dar H

出版信息

J Reprod Med. 1981 Jan;26(1):52-5.

PMID:7205814
Abstract

A 22;22 Robertsonian translocation was diagnosed in a husband whose wife had had six consecutive early spontaneous abortions and no normal progeny. With the new multiple-exposure photography (MEP) technique, an accurate, objective and documentary sperm analysis was performed. No abnormality of the essentially defective, genetically unbalanced sperms could be detected in regard to sperm count, motility, velocity and morphology. The only similar translocation previously reported in a male was associated with azoospermia. Recent literature correlating chromosomal aberrations and reproductive failure in the male is discussed in relation to the reported case. The importance of including the male partner in the cytogenetic investigation of couples with habitual abortion is stressed.

摘要

一名男性被诊断出患有22;22罗伯逊易位,其妻子连续六次早期自然流产,未生育正常后代。运用新的多重曝光摄影(MEP)技术,对精子进行了准确、客观且有记录的分析。在精子数量、活力、速度和形态方面,未检测到本质上有缺陷、基因不平衡精子的异常情况。此前报道的唯一一例男性类似易位病例与无精子症有关。结合该病例讨论了近期将染色体畸变与男性生殖失败相关联的文献。强调了在习惯性流产夫妇的细胞遗传学调查中纳入男性伴侣的重要性。

相似文献

1
Autosomal translocation in an apparently normospermic male as a cause of habitual abortion.一名精液参数看似正常的男性出现常染色体易位,作为习惯性流产的一个原因。
J Reprod Med. 1981 Jan;26(1):52-5.
2
[Cytogenetic study of peripheral lymphocyte culture in couples with habitual abortion].[习惯性流产夫妇外周血淋巴细胞培养的细胞遗传学研究]
Zentralbl Gynakol. 1991;113(19):1046-52, 1057-8.
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Cytogenetic findings in 318 couples with repeated spontaneous abortion: a review of experience in British Columbia.318对反复自然流产夫妇的细胞遗传学研究结果:不列颠哥伦比亚省经验回顾
Am J Med Genet. 1984 Mar;17(3):615-20. doi: 10.1002/ajmg.1320170310.
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Reproductive risk in mating between two translocation carriers: case report and review of the literature.两名易位携带者之间交配的生殖风险:病例报告及文献综述
Am J Med Genet. 1993 Jun 15;46(5):524-8. doi: 10.1002/ajmg.1320460513.
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[Balanced translocation t (3; 21) (q 11; q 21) as a cause of habitual abortions].
Tsitol Genet. 1977 Jan-Feb;11(1):74-6.
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[Cytogenetic findings in habitual abortion. Chromosomal analysis in 123 couples (author's transl)].习惯性流产的细胞遗传学发现。123对夫妇的染色体分析(作者译)
Wien Klin Wochenschr. 1980 Aug 29;92(16):575-8.
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Cytogenetic analysis of 688 couples experiencing multiple spontaneous abortions.对688对经历多次自然流产的夫妇进行细胞遗传学分析。
Am J Med Genet. 1988 Mar;29(3):549-56. doi: 10.1002/ajmg.1320290312.
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The importance of cytogenetic investigation of the couples with multiple spontaneous abortions and malformed offsprings.
Endocrinologie. 1979 Jan-Mar;17(1):17-22.
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[Cytogenetic study of 30 couples having had several spontaneous abortions].对30对有多次自然流产史的夫妇进行的细胞遗传学研究
Sem Hop. 1975 Jan 26;51(5):299-302.
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[Chromosomes and fertility. Translocation 13:15 and 13:18 and spontaneous abortion].[染色体与生育能力。13:15和13:18易位与自然流产]
Jugosl Ginekol Opstet. 1981 Jan-Apr;21(1-2):23-5.

引用本文的文献

1
De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case.一名复发性流产女性的新发平衡罗伯逊易位rob(22;22)(q10;q10):罕见病例
J Reprod Infertil. 2018 Jan-Mar;19(1):61-66.