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Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: A Case Report | Abstract

Journal of Research in Medical and Dental Science
eISSN No. 2347-2367 pISSN No. 2347-2545

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Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: A Case Report

Author(s): Jadhav Mayuri, Nikam Vasudha, Ghorpade Vijay, Patil Asha, Pote A J

Abstract

The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital disorder characterized by aplasia of the uterus and the upper part of vagina in an XX individual with normal development of secondary sexual characteristics. To help establish the best criteria for early diagnosis and treatment options for a comprehensive therapeutic approach to MRKH patients, we report the case of a 19-year-old woman who presented with primary amenorrhea. Correct evaluation of these patients and proper management is mandatory.

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