Volume : X, Issue : VI, June - 2020

MAYER ROKITANSKY-KUSTER-HAUSER SYNDROME: SYNDROME OF AGENESIS- A CASE REPORT

Dr. V. Dhanalakshmi, Dr. M. Kaavya

Abstract :

Mayer–Rokitansky–Kuster–Hauser syndrome is the complete failure in the development of the mullerian duct resulting in the absence of the fallopian tubes, uterus and most of the vagina .It affects atleast 1 in 4,500 women. The patients have normal female karyotype .Renal ectopy and agenesis, skeletal abnormalities, as well as cardiac abnormalities are associated. The MRKH syndrome has been linked with decreased galactose–1–phosphate uridyl transferase activity leading to increased galactose exposure. Here we report a case of MRKH syndrome in a 17yr old female who presented with primary amenorrhoea

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Article: Download PDF    DOI : 10.36106/ijar  

Cite This Article:

MAYER ROKITANSKY-KUSTER-HAUSER SYNDROME: SYNDROME OF AGENESIS- A CASE REPORT, Dr. V.DHANALAKSHMI, Dr. M.KAAVYA INDIAN JOURNAL OF APPLIED RESEARCH : Volume-10 | Issue-6 | June-2020

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