Suppr超能文献

与染色体平衡易位相关的复发性自发性流产:两例病例报告。

Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports.

机构信息

Key Laboratory of Cell Engineering in Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi, 563003, Guizhou, China.

The Engineering Research Center of Zunyi Precision Medical Detection and Birth Defects Prevention and Control, Affiliated Hospital of Zunyi Medical University, Zunyi, 563003, Guizhou, China.

出版信息

J Med Case Rep. 2021 May 24;15(1):270. doi: 10.1186/s13256-021-02848-9.

Abstract

BACKGROUND

Recurrent spontaneous abortion (RSA) is often idiopathic, but structural chromosomal abnormality is an important nosogenesis. Balanced translocations or inversions can lead to unbalanced gametes depending on the specific recombination and segregation patterns during meiosis. An unbalanced karyotype in the conceptus of a couple when one partner has a structural chromosomal abnormality may result in failure to implant, miscarriage, or ongoing pregnancy of a fetus with an unbalanced karyotype.

CASE PRESENTATION

We report two rare Han cases of RSA associated with balanced translocation of chromosomes. In case 1, a women who had had four spontaneous abortions, the karyotype was 46, XX, t (4;7) (q31;q22). In case 2, a women who had two spontaneous abortions and one stillborn fetus, the karyotype was 46, XX, t (3;15) (q12;p11.2), inv (5) (P13q13). The abnormal karyotype was not found in other chromosomes.

CONCLUSIONS

It is very important that couples with more than two miscarriages be provided with chromosomal analysis. Referring couples for karyotyping will rule out or confirm possible hereditary etiology and the source of chromosomal abnormalities in recurrent miscarriages.

摘要

背景

复发性自然流产(RSA)通常是特发性的,但结构染色体异常是一个重要的发病机制。平衡易位或倒位可能会导致非平衡配子,具体取决于减数分裂过程中的特定重组和分离模式。当一对夫妇中的一方存在结构染色体异常时,胚胎中的不平衡核型可能导致着床失败、流产或胎儿的不平衡核型持续妊娠。

病例介绍

我们报告了两例与染色体平衡易位相关的罕见汉族 RSA 病例。在病例 1 中,一名曾发生过四次自然流产的女性,其核型为 46,XX,t(4;7)(q31;q22)。在病例 2 中,一名曾发生过两次自然流产和一次死胎的女性,其核型为 46,XX,t(3;15)(q12;p11.2),inv(5)(P13q13)。其他染色体未发现异常核型。

结论

对于多次流产的夫妇,提供染色体分析非常重要。夫妻双方进行核型分析可以排除或确认可能的遗传性病因和复发性流产中染色体异常的来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd8/8142492/f61d0eaba6e3/13256_2021_2848_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验