Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female

Meyer–Rokitansky–Kuster–Hauser syndrome is a rare congenital abnormality occurring sporadically in females. It is the most common cause of primary amenorrhea. Affected persons usually appear normal on physical examination. This is a case of a 25-year-old woman who presented with primary amenorrhea a...

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Detalles Bibliográficos
Autores principales: Ajiboye, Akinyosoye D., Omokanye, Lukman O., Olatinwo, Abdulwaheed O., Biliaminu, Sikiru A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298376/
https://www.ncbi.nlm.nih.gov/pubmed/30787776
http://dx.doi.org/10.4103/1658-631X.204859
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author Ajiboye, Akinyosoye D.
Omokanye, Lukman O.
Olatinwo, Abdulwaheed O.
Biliaminu, Sikiru A.
author_facet Ajiboye, Akinyosoye D.
Omokanye, Lukman O.
Olatinwo, Abdulwaheed O.
Biliaminu, Sikiru A.
author_sort Ajiboye, Akinyosoye D.
collection PubMed
description Meyer–Rokitansky–Kuster–Hauser syndrome is a rare congenital abnormality occurring sporadically in females. It is the most common cause of primary amenorrhea. Affected persons usually appear normal on physical examination. This is a case of a 25-year-old woman who presented with primary amenorrhea and, subsequently, had diagnostic laparoscopy to confirm the diagnosis of Mullerian agenesis.
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spelling pubmed-62983762019-02-20 Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female Ajiboye, Akinyosoye D. Omokanye, Lukman O. Olatinwo, Abdulwaheed O. Biliaminu, Sikiru A. Saudi J Med Med Sci Case Report Meyer–Rokitansky–Kuster–Hauser syndrome is a rare congenital abnormality occurring sporadically in females. It is the most common cause of primary amenorrhea. Affected persons usually appear normal on physical examination. This is a case of a 25-year-old woman who presented with primary amenorrhea and, subsequently, had diagnostic laparoscopy to confirm the diagnosis of Mullerian agenesis. Medknow Publications & Media Pvt Ltd 2017 2017-04-20 /pmc/articles/PMC6298376/ /pubmed/30787776 http://dx.doi.org/10.4103/1658-631X.204859 Text en Copyright: © 2017 Saudi Journal of Medicine & Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Ajiboye, Akinyosoye D.
Omokanye, Lukman O.
Olatinwo, Abdulwaheed O.
Biliaminu, Sikiru A.
Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female
title Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female
title_full Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female
title_fullStr Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female
title_full_unstemmed Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female
title_short Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female
title_sort mullerian agenesis with primary amenorrhea: a case report of a normal phenotypic female
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298376/
https://www.ncbi.nlm.nih.gov/pubmed/30787776
http://dx.doi.org/10.4103/1658-631X.204859
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