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本文引用的文献

1
Birth of a boy after intracytoplasmic sperm injection using ejaculated spermatozoa from a nonmosaic klinefelter syndrome man with normal sperm motility: A case report.使用一名精子活力正常的非嵌合型克兰费尔特综合征男性射出的精子进行卵胞浆内单精子注射后诞下一名男婴:病例报告
Front Genet. 2022 Sep 23;13:989701. doi: 10.3389/fgene.2022.989701. eCollection 2022.
2
Microdissection testicular sperm extraction (micro-TESE) in men with infertility due to nonobstructive azoospermia: summary of current literature.非梗阻性无精子症导致不育的男性中显微睾丸精子提取术(micro-TESE):当前文献综述。
Int Urol Nephrol. 2021 Nov;53(11):2193-2210. doi: 10.1007/s11255-021-02979-4. Epub 2021 Aug 19.
3
Re: International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts, by T. Liehr.关于:《国际人类细胞遗传学或细胞基因组命名系统(ISCN):一些思考》,作者T. 利尔
Cytogenet Genome Res. 2021;161(5):225-226. doi: 10.1159/000516655. Epub 2021 Aug 18.
4
Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases.用于评估胎儿性染色体非整倍体的无创产前检测:45773例病例的回顾性研究
Mol Cytogenet. 2021 Jan 6;14(1):1. doi: 10.1186/s13039-020-00521-2.
5
European academy of andrology guidelines on Klinefelter Syndrome Endorsing Organization: European Society of Endocrinology.欧洲男科学会克莱恩费尔特综合征指南 支持机构:欧洲内分泌学会
Andrology. 2021 Jan;9(1):145-167. doi: 10.1111/andr.12909. Epub 2020 Oct 6.
6
Epigenetics and genomics in Klinefelter syndrome.克氏综合征的表观遗传学和基因组学。
Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):216-225. doi: 10.1002/ajmg.c.31802. Epub 2020 Jun 2.
7
Gonadal dysfunction and beyond: Clinical challenges in children, adolescents, and adults with 47,XXY Klinefelter syndrome.性腺功能障碍及其他:47,XXY 克氏综合征患儿、青少年和成人的临床挑战。
Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):302-312. doi: 10.1002/ajmg.c.31786. Epub 2020 May 16.
8
Novel insights on testicular volume and testosterone replacement therapy in Klinefelter patients undergoing testicular sperm extraction. A retrospective clinical study.关于行睾丸精子抽吸术的 Klinefelter 患者睾丸体积和睾酮替代治疗的新见解。一项回顾性临床研究。
Clin Endocrinol (Oxf). 2018 May;88(5):711-718. doi: 10.1111/cen.13572. Epub 2018 Mar 12.
9
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Endocr Rev. 2018 Aug 1;39(4):389-423. doi: 10.1210/er.2017-00212.
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Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism.克兰费尔特综合征(KS):遗传学、临床表型与性腺功能减退
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一例45岁男性的嵌合型克兰费尔特综合征罕见病例:通过射出精子实现成功活产——病例报告及文献综述

A rare case of mosaic Klinefelter syndrome in a 45-year-old man leading to successful live birth through ejaculated spermatozoa: a case report and literature review.

作者信息

Elzeiny Hossam, Agresta Franca, Stevens John, Gardner David K

机构信息

Melbourne IVF, Melbourne, VIC, Australia.

Royal Women's Hospital, Melbourne, VIC, Australia.

出版信息

Front Genet. 2023 Sep 13;14:1242180. doi: 10.3389/fgene.2023.1242180. eCollection 2023.

DOI:10.3389/fgene.2023.1242180
PMID:37779907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10533916/
Abstract

Men diagnosed with Klinefelter syndrome (KS) commonly exhibit non-obstructive azoospermia or rarely having sperm in their ejaculate, rendering them traditionally considered sterile prior to the introduction of intracytoplasmic sperm injection (ICSI). The presence of mosaic KS may mask the classical phenotype, resulting in underdiagnosis throughout their lifetime. Surgical sperm retrieval through Microdissection Testicular Sperm Extraction (Micro-TESE) combined with ICSI has become the gold standard approach, maximizing reproductive outcomes in these individuals. However, it is noteworthy that approximately 7% of men with KS may exhibit sperm in their ejaculate, providing an opportunity for them to achieve biological parenthood through ICSI. In this report, we present an exceptional case of a 45-year-old man with Mosaic KS and severe oligozoospermia who successfully achieved pregnancy utilizing ICSI with freshly ejaculated sperm. Remarkably, this case represents the oldest recorded instance of a man with Klinefelter syndrome fathering his own biological child using sperm derived from fresh ejaculate. Although this case is exceedingly rare, it underscores the critical importance of exhausting all possibilities to facilitate biological parenthood in men with KS before considering alternative options such as sperm donation or adoption. By recognizing the potential for successful conception using ejaculated sperm in this population, we can provide individuals with mosaic KS the opportunity to fulfill their desire for biological offspring.

摘要

被诊断患有克兰费尔特综合征(KS)的男性通常表现为非梗阻性无精子症,或者精液中极少有精子,这使得他们在卵胞浆内单精子注射(ICSI)技术出现之前,传统上被认为是不育的。嵌合型KS的存在可能会掩盖典型表型,导致他们一生都未被充分诊断。通过显微切割睾丸取精术(Micro-TESE)联合ICSI进行手术取精已成为金标准方法,能使这些患者的生殖结局最大化。然而,值得注意的是,约7%的KS男性精液中可能有精子,这为他们通过ICSI实现生育亲权提供了机会。在本报告中,我们介绍了一例特殊病例,一名45岁患有嵌合型KS且严重少精子症的男性,利用新鲜射出的精子通过ICSI成功受孕。值得注意的是,该病例是有记录以来年龄最大的克兰费尔特综合征男性利用新鲜射出精子生育自己亲生孩子的案例。尽管此病例极为罕见,但它强调了在考虑精子捐赠或收养等替代方案之前,穷尽一切可能性促进KS男性生育亲权的至关重要性。通过认识到该人群利用射出精子成功受孕的可能性,我们可以为嵌合型KS患者提供实现生育亲生后代愿望的机会。