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Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome
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...
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008953/ https://www.ncbi.nlm.nih.gov/pubmed/21206686 http://dx.doi.org/10.4103/0971-4065.73447 |
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author | Wani, M. M. Mir, S. A. |
author_facet | Wani, M. M. Mir, S. A. |
author_sort | Wani, M. M. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-3008953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-30089532011-01-04 Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome Wani, M. M. Mir, S. A. Indian J Nephrol Case Report 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. Medknow Publications 2010-10 /pmc/articles/PMC3008953/ /pubmed/21206686 http://dx.doi.org/10.4103/0971-4065.73447 Text en © Indian Journal of Nephrology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Wani, M. M. Mir, S. A. Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome |
title | Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome |
title_full | Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome |
title_fullStr | Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome |
title_full_unstemmed | Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome |
title_short | Chronic kidney disease in Mayer-Rokitansky-Kuster-Hauser Syndrome |
title_sort | chronic kidney disease in mayer-rokitansky-kuster-hauser syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008953/ https://www.ncbi.nlm.nih.gov/pubmed/21206686 http://dx.doi.org/10.4103/0971-4065.73447 |
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