Literature DB >> 23034780

Undetected sex chromosome aneuploidy by chromosomal microarray.

Keren Markus-Bustani, Yuval Yaron, Myriam Goldstein, Avi Orr-Urtreger, Shay Ben-Shachar.   

Abstract

We report on a case of a female fetus found to be mosaic for Turner syndrome (45,X) and trisomy X (47,XXX). Chromosomal microarray analysis (CMA) failed to detect the aneuploidy because of a normal average dosage of the X chromosome. This case represents an unusual instance in which CMA may not detect chromosomal aberrations. Such a possibility should be taken into consideration in similar cases where CMA is used in a clinical setting.
© 2012 John Wiley & Sons, Ltd.

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Year:  2012        PMID: 23034780     DOI: 10.1002/pd.3979

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  3 in total

1.  A new method to identify fetal sex and trisomy 21 from the amniocentesis of pregnant women.

Authors:  Junbei Xiang; Qian Wan; Mianxue Liu; Ruifeng Wang
Journal:  Hum Cell       Date:  2019-12-13       Impact factor: 4.174

2.  Clinical Selection of Prenatal Diagnostic Techniques Following Positive Noninvasive Prenatal Screening Results in Southwest China.

Authors:  Xiaosha Jing; Hongqian Liu; Qian Zhu; Sha Liu; Jianlong Liu; Ting Bai; Cechuan Deng; Tianyu Xia; Yunyun Liu; Jing Cheng; Xiang Wei; Lingling Xing; Yuan Luo; Quanfang Zhou; Lin Chen; Lingping Li; Jiamin Wang
Journal:  Front Genet       Date:  2022-01-28       Impact factor: 4.599

3.  The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis.

Authors:  MengZhe Hao; LeiLei Li; Han Zhang; LinLin Li; Ruizhi Liu; Yang Yu
Journal:  J Clin Lab Anal       Date:  2020-08-30       Impact factor: 3.124

  3 in total

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