MAYER-ROKITANSKY-KUSTER-HAUSER (MRKH) SYNDROME TYPE 2: ATYPICAL PRESENTATION OF RARE CASE

Authors

  • Ashok Nakum B. J. Medical College, Ahmedabad, Gujarat
  • Kesharmal Kumawat B. J. Medical College, Ahmedabad, Gujarat
  • Hiral Chauhan B. J. Medical College, Ahmedabad, Gujarat
  • Jayesh V Parikh B. J. Medical College, Ahmedabad, Gujarat

Keywords:

Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, Mullerian Defects, Urinary Tract Anomalies

Abstract

Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital malformation characterized by an absence of the vagina associated with a variable abnormality of the uterus and the urinary tract but functional ovaries. We are reporting atypical presentation of rare case. Patient had obstructed left inguinal hernia with genitourinary and skeletal deformity. Latter it diagnosed as Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome which is a rare disease.

Downloads

Published

2013-12-31

How to Cite

Nakum, A. ., Kumawat, K. ., Chauhan, H., & Parikh, J. V. . (2013). MAYER-ROKITANSKY-KUSTER-HAUSER (MRKH) SYNDROME TYPE 2: ATYPICAL PRESENTATION OF RARE CASE. National Journal of Medical Research, 3(04), 409–411. Retrieved from https://njmr.in/index.php/file/article/view/686

Issue

Vol. 3 No. 04 (2013)

Section

Case Report

License

Creative Commons License

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

Author/s retain the copyright of their article,  with first publication rights granted to Medsci Publications.