Mayer-Rokitansky-Kuster-Hauser Type I Syndrome - A Case Report

Authors

  • Sharma BB
  • Sharma S
  • Singh Y
  • Balesa J

DOI:

https://doi.org/10.32677/IJCR.2015.v01.i01.003

Keywords:

MRKH Syndrome, Mullerian agenesis, amenorrhoea, MRI

Abstract

Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome is not uncommon as this is a part of the Mullerian agenesis. This is
usually diagnosed during adolescent period when signs and symptoms of the ongoing changes in female body type are delayed. We present 17 years old adolescent female who presented with primary amenorrhoea as the normal menstruation did not start at puberty. She was diagnosed as MRKH Type I Syndrome on the basis of radiological investigations.

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Published

2020-10-01

Issue

Vol. 1 No. 1 (2015): January - March

Section

Case Report

License

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

How to Cite

Mayer-Rokitansky-Kuster-Hauser Type I Syndrome - A Case Report. (2020). Indian Journal of Case Reports, 1(1), 8-10. https://doi.org/10.32677/IJCR.2015.v01.i01.003