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最初分类为46,XY胚胎移植,最终妊娠产物为45,X——一例病例报告及不一致结果处理的综述

Initially categorized 46,XY embryo transfer ending with 45,X products of conception-a case report and a review of discordant result management.

作者信息

Singh Prapti, Snider Alyssa, Kayali Refik, Mancuso Abigail

机构信息

Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, University of Iowa, Iowa City, Iowa.

Igenomix, Torrance, California.

出版信息

F S Rep. 2024 May 22;5(3):328-332. doi: 10.1016/j.xfre.2024.05.006. eCollection 2024 Sep.

Abstract

OBJECTIVE

To report a case of an initially categorized euploid male embryo screened using preimplantation genetic testing (PGT) resulting in miscarriage and testing of products of conception consistent with Turner syndrome, and to discuss additional workup and considerations in cases of discrepancy.

DESIGN

Case report.

SETTING

University fertility clinic.

INTERVENTION

Frozen single embryo transfer of a euploid male embryo.

PATIENTS

A couple seeking procreative management for a female partner having a balanced translocation 46,XX,t(14;16)(q21;q21) diagnosed after the couple's previous child passed because of segmental duplication in chromosomes 14 and 16 and pursued in vitro fertilization treatment for PGT for structural rearrangements.

MAIN OUTCOME MEASURES

Miscarriage with discordant chromosomal microarray result.

RESULTS

Couple conceived with the transfer of a euploid male embryo. After the initial confirmation of pregnancy, repeat imaging indicated a missed abortion. Dilation and curettage were performed, and the products of conception were sent for chromosomal microarray. Results indicated Turner syndrome (45,X). Follow-up short tandem repeat analysis confirmed the products of conception were from the tested embryo. After reevaluation of the data, copy number variations below the reporting threshold for the sex chromosomes were observable and compatible with mosaic 45,X/46,XY.

CONCLUSIONS

The limitations of PGT should be kept in mind when counseling patients because of both the sample provided by biopsy, the sequencing platforms and the laboratory pipeline for diagnosis. We recommend that patients be counseled about these limitations and offered antenatal and postnatal testing as indicated. When discrepancies are seen after PGT, collaboration with the reference laboratory and additional testing with short tandem repeat analysis should be considered when possible.

摘要

目的

报告一例最初经植入前基因检测(PGT)筛查为整倍体男性胚胎,最终导致流产,且妊娠产物检测结果符合特纳综合征的病例,并讨论出现差异情况时的进一步检查及注意事项。

设计

病例报告。

地点

大学附属生育诊所。

干预措施

冷冻单胚胎移植一枚整倍体男性胚胎。

患者

一对夫妇,因女方存在平衡易位46,XX,t(14;16)(q21;q21),此前他们的孩子因14号和16号染色体节段重复而夭折,现寻求生育管理,为此女方接受体外受精并进行PGT以检测结构重排。

主要观察指标

流产且染色体微阵列结果不一致。

结果

该夫妇通过移植整倍体男性胚胎成功受孕。初次确认妊娠后,重复影像学检查提示稽留流产。行刮宫术,将妊娠产物送去进行染色体微阵列检测。结果显示为特纳综合征(45,X)。后续的短串联重复序列分析证实妊娠产物来自检测的胚胎。重新评估数据后,可观察到性染色体低于报告阈值的拷贝数变异,与嵌合型45,X/46,XY相符。

结论

在为患者提供咨询时应牢记PGT的局限性,这是由于活检提供的样本、测序平台以及诊断的实验室流程等多方面因素导致的。我们建议向患者说明这些局限性,并根据情况提供产前和产后检测。当PGT后出现差异时,应尽可能与参考实验室合作,并考虑进行短串联重复序列分析等额外检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/056d/11456636/982b0d021719/gr1.jpg

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