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 CASE REPORT
Year : 2010  |  Volume : 20  |  Issue : 4  |  Page : 214-216

Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome


Department of Medicine, Al-Amiri Hospital and Al Nafisi dialysis centre, Kuwait

Correspondence Address:
M M Wani
Nik Nax, 6 Poloview, Srinagar, India

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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0971-4065.73447

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Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by either absence or abnormalities of the mullerian structures. It is a rare disorder, resulting in complete or partial agenesis of the uterus and cervix and primary amenorrhea. It may rarely be associated with anomalies of the urinary tract, ovaries and skeleton. Renal failure secondary to chronic tubulo-interstitial disease has been reported. We report a case of MRKH syndrome presenting late with chronic kidney disease.






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Indian Journal of Nephrology
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Online since 20th Sept '07