Pregnancy in a woman with Kallmann-De Morsier syndrome: A case report.

IF 1.6 Q3 OBSTETRICS & GYNECOLOGY
Ibtissam Bellajdel, Fatima-Zahra Mounassib, Hafsa Taheri, Chaymae Rochdi, Hanane Saadi, Mohammed Choukri, Ahmed Mimouni
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引用次数: 0

Abstract

Kallmann syndrome is characterized by the combination of hypogonadotropic hypogonadism and anosmia. It is a clinically and genetically heterogeneous disorder. We report the case of ovarian stimulation in a woman with Kallmann-De Morsier syndrome, resulting in a pregnancy achieved through insemination, which progressed to term. The patient underwent cesarean section for a contracted pelvis and delivered a live female infant. Drawing upon a review of the literature on Kallmann-De Morsier syndrome, we discuss the role of follicle-stimulating hormone during the follicular phase, as well as criteria for monitoring ovarian stimulation.

Kallmann-De Morsier综合征妇女妊娠:1例报告。
Kallmann综合征以促性腺功能减退和嗅觉缺失相结合为特征。它是一种临床和遗传异质性疾病。我们报告的情况下卵巢刺激的妇女与卡尔曼-德莫尔西耶综合征,导致怀孕通过人工授精,这进展到足月。由于骨盆收缩,患者接受了剖宫产手术,生下了一名女婴。在回顾有关Kallmann-De Morsier综合征的文献后,我们讨论了促卵泡激素在卵泡期的作用,以及监测卵巢刺激的标准。
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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来源期刊
CiteScore
3.30
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0.00%
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