{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,31]],"date-time":"2026-08-31T05:22:52Z","timestamp":1788153772770,"version":"build-2803163510"},"reference-count":14,"publisher":"The Korean Society for Reproductive Medicine","issue":"3","license":[{"start":{"date-parts":[[2026,1,22]],"date-time":"2026-01-22T00:00:00Z","timestamp":1769040000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":["ecerm.org"],"crossmark-restriction":true},"short-container-title":["Clin Exp Reprod Med"],"published-print":{"date-parts":[[2026,9,1]]},"abstract":"<jats:p>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.<\/jats:p>","DOI":"10.5653\/cerm.2024.07528","type":"journal-article","created":{"date-parts":[[2026,1,21]],"date-time":"2026-01-21T23:45:36Z","timestamp":1769039136000},"page":"307-310","update-policy":"https:\/\/doi.org\/10.5653\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Pregnancy in a woman with Kallmann-De Morsier syndrome: A case 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