Saudi Journal of Medicine and Medical Sciences

CASE REPORT
Year
: 2017  |  Volume : 5  |  Issue : 2  |  Page : 160--162

Mullerian agenesis with primary amenorrhea: A case report of a normal phenotypic female


Akinyosoye D Ajiboye1, Lukman O Omokanye1, Abdulwaheed O Olatinwo1, Sikiru A Biliaminu2 
1 Department of Obstetrics and Gynaecology, College of Health Sciences, University of Ilorin, Ilorin, Nigeria
2 Department of Chemical Pathology and Immunology, College of Health Sciences, University of Ilorin, Ilorin, Nigeria

Correspondence Address:
Lukman O Omokanye
Department of Obstetrics and Gynaecology, College of Health Sciences, University of Ilorin, Ilorin
Nigeria

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.


How to cite this article:
Ajiboye AD, Omokanye LO, Olatinwo AO, Biliaminu SA. Mullerian agenesis with primary amenorrhea: A case report of a normal phenotypic female.Saudi J Med Med Sci 2017;5:160-162


How to cite this URL:
Ajiboye AD, Omokanye LO, Olatinwo AO, Biliaminu SA. Mullerian agenesis with primary amenorrhea: A case report of a normal phenotypic female. Saudi J Med Med Sci [serial online] 2017 [cited 2021 Apr 17 ];5:160-162
Available from: https://www.sjmms.net/article.asp?issn=1658-631X;year=2017;volume=5;issue=2;spage=160;epage=162;aulast=Ajiboye;type=0