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精液参数正常且具备受孕能力的非嵌合型克兰费尔特综合征。

Non-mosaic Klinefelter syndrome with normal semen parameters and ability to conceive.

作者信息

Ma WenHan, Li ShuHua, Chen YuJun, Ma Ling, Lei JunHao

机构信息

Center for Reproductive Medicine, Zhongnan Hospital of Wuhan University, 430071, Wuhan, Hubei, P.R. China.

Clinical Medicine Research Centre of Reproductive Health and Birth Health in Wuhan City, Wuhan, 430071, Hubei, China.

出版信息

J Assist Reprod Genet. 2025 Sep 15. doi: 10.1007/s10815-025-03662-8.

Abstract

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.

摘要

背景

非嵌合型47,XXY(克兰费尔特综合征,KS)男性很少能保持正常精子发生。在此,我们描述一名43岁生育能力正常的男性(既往自然受孕,精液参数正常),这对传统表型模式提出了挑战。

目的

报告一例具有生育能力且精液正常的罕见非嵌合型47,XXY病例,重新定义经典表型规范。

材料与方法

我们对一对夫妇(男性,非嵌合型47,XXY;女性,核型正常)进行了两个PGT-A周期的观察性研究。数据包括精液分析、生殖系统超声检查、内分泌概况和胚胎遗传学诊断。

结果

使用新鲜/解冻精子进行的两个PGT-A周期产生了3个囊胚:第一个周期有2个非整倍体囊胚(3BC;6BC),第二个周期有1个未检测的囊胚(4BC)。由于成本限制,患者在第二个周期拒绝进行整倍体检测。对未检测的囊胚进行了解冻胚胎移植(FET),但未怀孕。

结论

本研究呈现了一例范式转变的病例,即男性伴侣患有非嵌合型KS但具有生育潜力的夫妇成功进行了辅助生殖。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)对生殖内分泌功能进行全面评估,(2)对睾丸微环境进行分子特征分析,以及(3)对非典型KS表现的生育潜力进行纵向评估。

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