非嵌合克氏综合征,精液参数正常,受孕能力正常。

IF 2.7 3区 医学 Q2 GENETICS & HEREDITY
WenHan Ma, ShuHua Li, YuJun Chen, Ling Ma, JunHao Lei
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引用次数: 0

摘要

背景:非嵌合47,XXY (Klinefelter综合征,KS)男性很少保留精子发生。在这里,我们描述了一个43岁的男性完整的生育能力(先前的自然受孕,正常的精液参数),挑战传统的表型范式。目的:报告一例保留生育能力和正常精子症的异常非马赛克病例,重新定义经典表型规范。材料和方法:我们对一对夫妇(男性,非马赛克47,XXY;女性,正常核型)进行了两次PGT-A周期的观察研究。数据包括精液分析、生殖系统超声检查、内分泌谱和胚胎遗传诊断。结果:使用新鲜/解冻精子的两个PGT-A周期产生三个囊胚:第一个周期(公元前3BC;公元前6BC)产生两个非整倍体囊胚,第二个周期(公元前4BC)产生一个未经测试的囊胚。由于费用限制,患者拒绝了第二周期的整倍体检测。用未经测试的囊胚进行解冻胚胎移植(FET),结果没有怀孕。结论:本研究提出了一个范式转移的案例,成功的辅助生殖在一对夫妇,其中男性伴侣有保留生育潜力的非马赛克KS。我们的研究结果挑战了关于KS患者自然受孕的传统假设,并强调需要:(1)生殖内分泌功能的综合评估,(2)睾丸微环境的分子特征,以及(3)非典型KS表现的生育潜力的纵向评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-mosaic Klinefelter syndrome with normal semen parameters and ability to conceive.

Background: Non-mosaic 47,XXY (Klinefelter syndrome, KS) males rarely retain preserved spermatogenesis. Here, we describe a 43-year-old man with intact fertility (prior natural conception, normal semen parameters), challenging conventional phenotypic paradigms.

Objectives: To report an exceptional non-mosaic 47,XXY case with preserved fertility and normozoospermia, redefining classic phenotyping norms.

Materials and methods: We conducted an observational study of a couple (male, non-mosaic 47,XXY; female, normal karyotype) undergoing two PGT-A cycles. Data included semen analyses, reproductive system ultrasonography, endocrine profiles, and embryo genetic diagnostics.

Results: Two PGT-A cycles using fresh/thawed sperm yielded three blastocysts: two aneuploid blastocysts in the first cycle (3BC; 6BC) and one untested blastocyst in the second cycle (4BC). Due to cost constraints, the patient declined euploidy testing in the second cycle. A thawed embryo transfer (FET) was performed with the untested blastocyst, resulting in no pregnancy.

Conclusion: This study presents a paradigm-shifting case of successful assisted reproduction in a couple where the male partner has non-mosaic KS with preserved fertility potential. Our findings challenge conventional assumptions about natural conception in KS patients and underscore the need for: (1) comprehensive evaluation of reproductive endocrine function, (2) molecular characterization of the testicular microenvironment, and (3) longitudinal assessment of fertility potential in atypical KS presentations.

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来源期刊
CiteScore
5.70
自引率
9.70%
发文量
286
审稿时长
1 months
期刊介绍: The Journal of Assisted Reproduction and Genetics publishes cellular, molecular, genetic, and epigenetic discoveries advancing our understanding of the biology and underlying mechanisms from gametogenesis to offspring health. Special emphasis is placed on the practice and evolution of assisted reproduction technologies (ARTs) with reference to the diagnosis and management of diseases affecting fertility. Our goal is to educate our readership in the translation of basic and clinical discoveries made from human or relevant animal models to the safe and efficacious practice of human ARTs. The scientific rigor and ethical standards embraced by the JARG editorial team ensures a broad international base of expertise guiding the marriage of contemporary clinical research paradigms with basic science discovery. JARG publishes original papers, minireviews, case reports, and opinion pieces often combined into special topic issues that will educate clinicians and scientists with interests in the mechanisms of human development that bear on the treatment of infertility and emerging innovations in human ARTs. The guiding principles of male and female reproductive health impacting pre- and post-conceptional viability and developmental potential are emphasized within the purview of human reproductive health in current and future generations of our species. The journal is published in cooperation with the American Society for Reproductive Medicine, an organization of more than 8,000 physicians, researchers, nurses, technicians and other professionals dedicated to advancing knowledge and expertise in reproductive biology.
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