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Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports
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 yea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205315/ https://www.ncbi.nlm.nih.gov/pubmed/30410807 http://dx.doi.org/10.1155/2018/9294650 |
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author | Topdagi Yilmaz, Emsal Pinar Yapca, Omer Erkan Topdagi, Yunus Emre Kaya Topdagi, Seray Kumtepe, Yakup |
author_facet | Topdagi Yilmaz, Emsal Pinar Yapca, Omer Erkan Topdagi, Yunus Emre Kaya Topdagi, Seray Kumtepe, Yakup |
author_sort | Topdagi Yilmaz, Emsal Pinar |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6205315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-62053152018-11-08 Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports Topdagi Yilmaz, Emsal Pinar Yapca, Omer Erkan Topdagi, Yunus Emre Kaya Topdagi, Seray Kumtepe, Yakup Case Rep Obstet Gynecol Case Report 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. Hindawi 2018-10-15 /pmc/articles/PMC6205315/ /pubmed/30410807 http://dx.doi.org/10.1155/2018/9294650 Text en Copyright © 2018 Emsal Pinar Topdagi Yilmaz et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Topdagi Yilmaz, Emsal Pinar Yapca, Omer Erkan Topdagi, Yunus Emre Kaya Topdagi, Seray Kumtepe, Yakup Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports |
title | Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports |
title_full | Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports |
title_fullStr | Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports |
title_full_unstemmed | Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports |
title_short | Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports |
title_sort | spontaneous ovarian hyperstimulation syndrome with fsh receptor gene mutation: two rare case reports |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205315/ https://www.ncbi.nlm.nih.gov/pubmed/30410807 http://dx.doi.org/10.1155/2018/9294650 |
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