Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2017 May-Aug;5(2):160-162.
doi: 10.4103/1658-631X.204859. Epub 2017 Apr 20.

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

Akinyosoye D Ajiboye  1 , Lukman O Omokanye  1 , Abdulwaheed O Olatinwo  1 , Sikiru A Biliaminu  2
Affiliations
Case Reports

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

Akinyosoye D Ajiboye et al. Saudi J Med Med Sci. 2017 May-Aug.

Abstract
in English, Arabic

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.

ملخص البحث: تعتبر متلازمة (Meyer–Rokitansky–Kuster–Hauser (MRKH من الحالات النادرة التي تحدث بشكل متقطع لدى النساء. وهي من أكثر أسباب انقطاع الطمث الأولى. تبدو النساء المصابات بهذه المتلازمة طبيعيات عند الفحص السريري. يعرض الباحثون حالة لسيدة في الخامسة والعشرين من العمر تعاني من انقطاع طمث أولي. تم تشخيص الحالة بواسطة تنظير البطن التشخيصي على أنها ناتجة عن عدم تخلـــــق مولـــــــــر (Mullerian agenesis).

Keywords: Laparoscopy; Mayer-Rokitansky-Kuster-Hauser syndrome; Mullerian agenesis; primary amenorrhea.

PubMed Disclaimer

Conflict of interest statement

There are no conflicts of interest.

Figures

Figure 1
Figure 1
Operative findings: Absent uterus with blind ended vagina, grossly normal fallopian tubes and ovaries with evidence of follicular activities.
See this image and copyright information in PMC

Similar articles

See all similar articles

Cited by

References

    1. Manfroi RG, Chagas LA, Leal R, Cunha AL, Djahjah MC. Mayer-Rokitansky-Kuster-Hauser syndrome: A case report and literature review. Radiol Bras. 2011;44:192–4.
    1. Sultan C, Biason-Lauber A, Philibert P. Mayer-Rokitansky-Kuster-Hauser syndrome: Recent clinical and genetic findings. Gynecol Endocrinol. 2009;25:8–11. - PubMed
    1. Parikh R, Nakum K, Kadikar G, Gokhle A. Mullerian anomalies: A cause of primary amenorrhea. Int J Reprod Contracept Obstet Gynecol. 2013;2:393–7.
    1. Evans TN, Poland ML, Boving RL. Vaginal malformations. Am J Obstet Gynecol. 1981;141:910–20. - PubMed
    1. Guerrier D, Mouchel T, Pasquier L, Pellerin I. The Mayer-Rokitansky-Kuster-Hauser syndrome (congenital ansence of uterus and vagina)-phenotypic manifestations and genetic approaches. J Negat Results Biomed. 2006;5:1. - PMC - PubMed

Publication types