Successful ART outcome in a woman with McCune-Albright syndrome: a case report and literature review

被引:1
作者
Pirtea, Paul [1 ]
Haggerty, Estelle [1 ]
Hagege, Estelle [1 ]
Tran, Chloe [1 ]
de Ziegler, Dominique [1 ]
Farabet, Clemence [1 ]
Filali, Meryem [1 ]
Poulain, Marine [1 ]
Ayoubi, Jean Marc [1 ]
机构
[1] Foch Hosp, Dept Obstet Gynecol & Reprod Med, F-92150 Suresnes, France
关键词
McCune-Albright syndrome; Infertility; ART; In vitro maturation IVM; STIMULATORY G-PROTEIN; ACTIVATING MUTATIONS; FIBROUS DYSPLASIA; DYNAMICS; ABNORMALITIES; OOPHORECTOMY; PUBERTY; GIRLS; BONE;
D O I
10.1007/s10815-023-02844-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
McCune-Albright syndrome (MAS) is a rare genetic disease affecting multiple organs, including endocrine tissues. This endocrinopathy is sometimes responsible for infertility, as it may induce an independent functioning of the ovaries leading to anovulatory cycles. This case report describes the infertility journey of a 22-year-old female who had early puberty and irregular periods with high estrogen and progesterone levels, low FSH and LH (on day 3 of her menstrual cycle), and a multi-cystic right ovary. She received several infertility treatments: initially in vitro oocyte maturation (IVM) followed by cyst transvaginal ultrasound-guided aspiration, all unsuccessful. A right hemi-ovariectomy was performed that eventually restored regular cycles and made it possible to perform ovarian stimulation (OS) and in vitro fertilization (IVF). Live birth was obtained after the first embryo transfer.
引用
收藏
页码:1669 / 1675
页数:7
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