Guo Zhenglong, Kang Bing, Wu Dong, Xiao Hai, Hao Leilei, Hao Bingtao, Liao Shixiu
Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, National Health Commission Key Laboratory of Birth Defects Prevention, Medical Genetic Institute of Henan Province, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou, China.
School of Medicine, People's Hospital of Henan University, Henan University, Zhengzhou, China.
Front Genet. 2022 Feb 3;12:740415. doi: 10.3389/fgene.2021.740415. eCollection 2021.
To report a rare case in which an IVF-ET twin pregnancy gave birth to a partial trisomy 21 chimera girl. Case report. University hospital. A girl with partial trisomy 21 mosaicism after fertilization and embryo transfer. fertilization (IVF) and embryo transfer (ET). Karyotype analysis, Copy Number Variation sequencing (CNV-seq), stLFR-WGS, and Short Tandem Repeat (STR) analysis. Being assisted with IVF and EF technology, the couple successfully gave birth to twin sisters at 37 weeks of gestational age. The NonInvasive Prenatal Testing (NIPT) and Nuchal Translucency (NT) examination showed no detectable genetic abnormalities during pregnancy. However, the younger infant displayed growth retardation and feeding difficulties after birth, which was not observed in her twin sister. Further genetic counseling and diagnosis suggested that she is a Chimera with complex partial trisomy 21. The stLFR-WGS assay showed multiple CNV variations in Chr21 and STR analysis confirmed the paternal origin of the additional fragments. It is rare for IVF-ET-assisted twin pregnancy to give birth to a girl with a complex combination of abnormal Chr21, which might result from paternal chromosome rearrangement during meiosis and mitosis.
报告一例罕见病例,体外受精-胚胎移植(IVF-ET)双胎妊娠分娩出一名21号染色体部分三体嵌合体女孩。病例报告。大学医院。一名在受精和胚胎移植后患有21号染色体部分三体嵌合体的女孩。受精(IVF)和胚胎移植(ET)。核型分析、拷贝数变异测序(CNV-seq)、单倍型长片段读取全基因组测序(stLFR-WGS)和短串联重复序列(STR)分析。这对夫妇通过IVF和ET技术辅助,在孕37周时成功分娩出一对双胞胎姐妹。无创产前检测(NIPT)和颈项透明层(NT)检查显示孕期未检测到基因异常。然而,较小的婴儿出生后出现生长发育迟缓及喂养困难,其双胞胎姐姐未出现此情况。进一步的遗传咨询和诊断表明她是一名患有复杂21号染色体部分三体的嵌合体。stLFR-WGS检测显示21号染色体存在多个拷贝数变异,STR分析证实额外片段来自父亲。IVF-ET辅助双胎妊娠分娩出一名具有复杂21号染色体异常组合的女孩极为罕见,这可能是由于减数分裂和有丝分裂过程中父源染色体重排所致。