Why Turner patients with 45, X monosomy should not be excluded from fertility preservation services.

M J Schleedoorn, K Fleischer, Ddm Braat, Ajm Oerlemans, Aaem van der Velden, R Peek
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引用次数: 3

Abstract

In this case report, we highlight the practical dilemma, i.e. to perform ovarian tissue cryopreservation surgery in a 45, X Turner Syndrome patient or not, by reporting on the presence of follicles in a 13-year-old female diagnosed with 45, X monosomy and an unmeasurable anti-müllerian hormone serum level. We compare our results with previous research, highlight the challenges we faced in this case and provide recommendations for daily practice. Hereby, we demonstrate that excluding certain subgroups of Turner Syndrome patients (e.g. monosomy patients, and/or girls with an anti-müllerian hormone level below 2.0 ng/l) may be premature, especially based on the current state of published research data. This practical example of a challenging dilemma in the counselling of Turner Syndrome patients for fertility preservation is of interest for clinicians involved in fertility counselling and Turner Syndrome care.

Abstract Image

Abstract Image

Abstract Image

为什么有45,X染色体的特纳患者不应该被排除在生育保留服务之外。
在本病例报告中,我们通过报道一名诊断为45x单体且血清抗勒氏激素水平无法测量的13岁女性的卵泡存在,强调了实际困境,即是否对45x特纳综合征患者进行卵巢组织冷冻保存手术。我们将我们的结果与之前的研究进行比较,强调我们在这个案例中面临的挑战,并为日常实践提供建议。因此,我们证明,排除特纳综合征患者的某些亚群(如单体患者和/或抗勒氏杆菌激素水平低于2.0 ng/l的女孩)可能为时过早,特别是基于目前已发表的研究数据。这是一个具有挑战性的困境的实际例子,在咨询特纳综合征患者的生育能力保存是有兴趣的临床医生参与生育咨询和特纳综合征护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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