Table of Contents

2016 Month : December Volume : 2 Issue : 2 Page : 15-17

MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME - A RARE CASE OF UTERINE AND BILATERAL OVARIAN AGENESIS.

Lavanya N1, Seetha Pramila V. V2, Nagesh R3, Anil Kumar Shukla4

Corresponding Author:
Dr. Anil Kumar Shukla,
# 77, Himagiri Apartment,
Flat 4C, 15th Cross,
4th Main, Malleswaram,
Bangalore-560055,
Karnataka.
E-mail: shookla2007@yahoo.co.in

ABSTRACT

BACKGROUND

Meyer-Rokitansky-Kuster-Hauser syndrome belongs to Class 1 Mullerian duct anomalies characterised by uterine anomalies including agenesis, hypoplasia or duplication.

CASE REPORT

we are presenting a case of a 19-year-old female patient with primary amenorrhoea and absence of bilateral breasts. Ultrasound and MRI pelvis were done.

CONCLUSION

MRI is an excellent modality to demonstrate the uterine, ovarian and renal anomalies that may be associated with Meyer-Rokitansky-Kuster-Hauser syndrome.

KEYWORDS

Mullerian ducts, primary amenorrhoea, dyspareunia.

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