![](/images/graphics-bg.png)
Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports
Joint Authors
Yapca, Omer Erkan
Yilmaz, Emsal Pinar Topdagi
Kumtepe, Yakup
Topdagi, Yunus Emre
Topdagi, Seray Kaya
Source
Case Reports in Obstetrics and Gynecology
Issue
Vol. 2018, Issue 2018 (31 Dec. 2018), pp.1-5, 5 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2018-10-15
Country of Publication
Egypt
No. of Pages
5
Main Subjects
Abstract EN
Development of ovarian hyperstimulation syndrome (OHSS) is very rare in a spontaneous ovulatory cycle and it is usually seen during pregnancy.
In the etiology of OHSS, higher hCG (molar pregnancies or multiple pregnancies) and thyroid-stimulating hormone (TSH) levels have been accused.
In recent years, some follicle-stimulating hormone (FSH) receptor (FSHR) gene mutations have been described in patients with OHSS in the first trimester with normal hCG levels.
Herein, we report two cases of FSHR gene mutation during the investigation of the etiology of spontaneous OHSS.
Although OHSS is typically associated with ovulation induction, it should be kept in mind that this condition may also develop in spontaneous pregnancies.
American Psychological Association (APA)
Yilmaz, Emsal Pinar Topdagi& Yapca, Omer Erkan& Topdagi, Yunus Emre& Topdagi, Seray Kaya& Kumtepe, Yakup. 2018. Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports. Case Reports in Obstetrics and Gynecology،Vol. 2018, no. 2018, pp.1-5.
https://search.emarefa.net/detail/BIM-1146013
Modern Language Association (MLA)
Yilmaz, Emsal Pinar Topdagi…[et al.]. Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports. Case Reports in Obstetrics and Gynecology No. 2018 (2018), pp.1-5.
https://search.emarefa.net/detail/BIM-1146013
American Medical Association (AMA)
Yilmaz, Emsal Pinar Topdagi& Yapca, Omer Erkan& Topdagi, Yunus Emre& Topdagi, Seray Kaya& Kumtepe, Yakup. Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports. Case Reports in Obstetrics and Gynecology. 2018. Vol. 2018, no. 2018, pp.1-5.
https://search.emarefa.net/detail/BIM-1146013
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1146013