AUTHOR=Ma Na , Zhu Zhenhua , Hu Jiancheng , Pang Jialun , Yang Shuting , Liu Jing , Chen Jing , Tang Wanglan , Kuang Haiyan , Hu Rong , Li Zhuo , Wang Hua , Peng Ying , Xi Hui TITLE=Case report: Detection of fetal trisomy 9 mosaicism by multiple genetic testing methods: Report of two cases JOURNAL=Frontiers in Genetics VOLUME=14 YEAR=2023 URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2023.1121121 DOI=10.3389/fgene.2023.1121121 ISSN=1664-8021 ABSTRACT=
Chromosomal mosaicism remains a perpetual diagnostic and clinical dilemma. In the present study, we detected two prenatal trisomy 9 mosaic syndrome cases by using multiple genetic testing methods. The non-invasive prenatal testing (NIPT) results suggested trisomy 9 in two fetuses. Karyotype analysis of amniocytes showed a high level (42%–50%) of mosaicism, and chromosomal microarray analysis (CMA) of uncultured amniocytes showed no copy number variation (CNV) except for large fragment loss of heterozygosity. Ultrasound findings were unmarkable except for small for gestational age. In Case 1, further umbilical blood puncture confirmed 22.4% and 34% trisomy 9 mosaicism by CMA and fluorescent