2015Int J GenetRequires access

Karyotype analysis on 279 couples with recurrent spontaneous abortion in Xinjiang

Cairong Zhang, Min Guo

Open publisher page 0 citations

Abstract

Objective To analyze the correlation of abnormal karyotypes with recurrent spontaneous abortion. Methods The chromosomal karyotypes were examined in 279 couples with spontaneous abortion history by using peripheral blood lymphocyte culture and G banding. Results 151 cases of 279 couples were abnormal in karyotype, with an abnormal rate of 27.1%. Among them, there were 12% chromosome structural aberrations (18/151) including 11 translocations, five inversions, one insertion and one deletion and 88.1% chromosome polymorphism (133/151) consisting of 108 Y chromosome and 25 other chromosome variations. Conclusion Y chromosome polymorphism is a significant genetic factor resulting in recurrent spontaneous abortion. Additionally, the balanced translocation, inversion and polymorphism also have correlations with spontaneous abortion. Their correlations should be further studied to provide reliable data for genetic counseling and eugenics. Key words: Recurrent spontaneous abortion; Chromosome; Abnormal karyotype

About this research paper

What this paper is about

Objective To analyze the correlation of abnormal karyotypes with recurrent spontaneous abortion. Methods The chromosomal karyotypes were examined in 279 couples with spontaneous abortion history by using peripheral blood lymphocyte culture and G banding. Results 151 cases of 279 couples were abnormal in karyotype, with an abnormal rate of 27.1%. Among them, there were 12% chromosome structural aberrations (18/151) including 11 translocations, five inversions, one insertion and one deletion and 88.1% chromosome polymorphism (133/151) consisting of 108 Y chromosome and 25 other chromosome variations. Conclusion Y chromosome polymorphism is a significant genetic factor resulting in recurrent spontaneous abortion. Additionally, the balanced translocation, inversion and polymorphism also have correlations with spontaneous abortion. Their correlations should be further studied to provide reliable data for genetic counseling and eugenics. Key words: Recurrent spontaneous abortion; Chromosome; Abnormal karyotype

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To analyze the correlation of abnormal karyotypes with recurrent spontaneous abortion. Methods The chromosomal karyotypes were examined in 279 couples with spontaneous abortion history by using peripheral blood lymphocyte culture and G banding. Results 151 cases of 279 couples were abnormal in karyotype, with an abnormal rate of 27.1%. Among them, there were 12% chromosome structural aberrations (18/151) including 11 translocations, five inversions, one insertion and one deletion and 88.1% chromosome polymorphism (133/151) consisting of 108 Y chromosome and 25 other chromosome variations. Conclusion Y chromosome polymorphism is a significant genetic factor resulting in recurrent spontaneous abortion. Additionally, the balanced translocation, inversion and polymorphism also have correlations with spontaneous abortion. Their correlations should be further studied to provide reliable data for genetic counseling and eugenics. Key words: Recurrent spontaneous abortion; Chromosome; Abnormal karyotype

Key concepts: Karyotype, Abortion, Chromosomal translocation, Chromosomal inversion, Genetics, Chromosome, Biology, Pregnancy

Related papers

Back to paper searchBrowse research topicsOriginal source
Karyotype analysis on 279 couples with recurrent spontaneous abortion in Xinjiang — Research Paper | ScholarLens