Evidence map›Paper›PMID 42050570›Full record

ArticleMolecular cytogenetics2026

A ten-year follow up case report on monochorionic dizygotic twins with confined blood chimerism of 47,XY,+21/46,XX.

Mengjie Shen, Huaying Ren, Ting Chen, Ke Chen

Abstract read
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Article in Molecular cytogenetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Mengjie ShenChongqing Key Laboratory of Human Embryo Engineering, Center of Reproductive Medicine, Women and Children's Hospital of Chongqing Medical University, Chongqing, 400013, China.
Huaying RenChongqing Key Laboratory of Human Embryo Engineering, Center of Reproductive Medicine, Women and Children's Hospital of Chongqing Medical University, Chongqing, 400013, China.
Ting ChenChongqing Key Laboratory of Human Embryo Engineering, Center of Reproductive Medicine, Women and Children's Hospital of Chongqing Medical University, Chongqing, 400013, China.
Ke ChenChongqing Key Laboratory of Human Embryo Engineering, Center of Reproductive Medicine, Women and Children's Hospital of Chongqing Medical University, Chongqing, 400013, China. johnkye@163.com.

Funding

Research and application of AI assessment technology for human oocyte and embryo quality in in vitro fertilization 82371728Research and development of AI assessment technology for human embryo quality in in vitro and quality evaluation No. CSTB2022TIAD-KPX0146
6 · The paper itself

Abstract

backgroundOnly ten patients with both trisomy 21 and normal karyotypes have been documented, including four singleton patients and three sets of twins. Among these twins, two were monochorionic dizygotic: one pair was terminated at 18 weeks, and the other was followed for two years. CASE PRESENTATION: A 38-year-old woman conceived through in vitro fertilization. Ultrasound examinations confirmed monochorionic twins. Standard karyotyping of peripheral blood cells from the twins revealed 47,XY,+21/46,XX chimerism, with a predominance of the 46,XX line. Single nucleotide polymorphism microarray analysis of oral mucosa cells identified a single cell line (46,XX) in the twin girl and a single cell line (47,XY,+21) in the twin boy. Over a decade of follow-up, the twins exhibited normal development, including hormonal values and external genitalia. While the twin boy exhibited a typical Down Syndrome phenotype.

conclusionsMonochorionic dizygotic (MCDZ) twins, though rare, can occur in assisted reproductive technology (ART) pregnancies, possibly due to blastocyst fusion or other mechanisms. These cases may be associated with confined blood chimerism (CBC) and monochorionic complications, despite genetic discordance between the twins. MCDZ twinning presents unique diagnostic and management challenges. For monochorionic dizygotic twins, early determination of zygosity and chorionicity is essential. Timely diagnosis, multidisciplinary care-including maternal-fetal medicine, medical genetics, and neonatology-and individualized counseling are critical components of management. Additionally, the mechanisms and long-term effects of intrauterine cell trafficking-especially concerning gonadal development-remain areas requiring further research.

Indexed as

ChimerismDown SyndromeIn vitro fertilizationMonochorionic dizygotic twins

Identifiers

PMID42050570
PMCPMC13267377

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