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Type 2 Mayer-Rokitansky-Kusner-Hauser syndrome

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Case Report

Author Details : Manju Agarwal, Somya Mathur*

Volume : 7, Issue : 3, Year : 2020

Article Page : 448-450

https://doi.org/10.18231/j.ijogr.2020.096

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Abstract

A 28-year-old married nulligravida presented with primary amenorrhea. There was no significant family
history of similar complaints. Her secondary sexual characters were well developed with hypoplastic
vagina. Ultrasonography of abdomen and pelvis revealed the absence of uterus and the right kidney. The
patient had normal 46, XX Karyotype.
She was diagnosed as a case of Type 2 MRKH after diagnostic laparoscopy. MRKH is very commonly
associated with renal agenesis. It had a huge psychological impact in the women and her family. The
patient was advised vaginoplasty, and surrogacy or child adoption as an option.

Keywords: MRKH, Primary ammenorhea, Renal agenesis.

How to cite : Agarwal M , Mathur S , Type 2 Mayer-Rokitansky-Kusner-Hauser syndrome. Indian J Obstet Gynecol Res 2020;7(3):448-450

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