| CASE REPORT |
|
| Year : 2010 | Volume
: 20
| Issue : 4 | Page : 214-216 |
Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome
MM Wani, SA Mir
Department of Medicine, Al-Amiri Hospital and Al Nafisi dialysis centre, Kuwait
Correspondence Address:
M M Wani
Nik Nax, 6 Poloview, Srinagar, India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0971-4065.73447
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.
[FULL TEXT] [PDF]*
|
|
Editorial Board
