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Marginal donor kidney in a marginal recipient: Five year follow-up
The widening gap between demand and supply of organs became apparent as organ shortage became more severe. Organs previously considered unsuitable for transplantation are currently being used. Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disease characterized by slow progress...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2931124/ https://www.ncbi.nlm.nih.gov/pubmed/20835327 http://dx.doi.org/10.4103/0971-4065.65306 |
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author | Bahadur, M. M. Binnani, P. Gupta, R. Pattewar, S. |
author_facet | Bahadur, M. M. Binnani, P. Gupta, R. Pattewar, S. |
author_sort | Bahadur, M. M. |
collection | PubMed |
description | The widening gap between demand and supply of organs became apparent as organ shortage became more severe. Organs previously considered unsuitable for transplantation are currently being used. Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disease characterized by slow progressive cystic changes and deterioration of renal function. We provide our experience with an ADPKD patient who received a kidney from 38-year-old deceased donor ADPKD-affected kidney for renal transplantation. |
format | Text |
id | pubmed-2931124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-29311242010-09-10 Marginal donor kidney in a marginal recipient: Five year follow-up Bahadur, M. M. Binnani, P. Gupta, R. Pattewar, S. Indian J Nephrol Case Report The widening gap between demand and supply of organs became apparent as organ shortage became more severe. Organs previously considered unsuitable for transplantation are currently being used. Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disease characterized by slow progressive cystic changes and deterioration of renal function. We provide our experience with an ADPKD patient who received a kidney from 38-year-old deceased donor ADPKD-affected kidney for renal transplantation. Medknow Publications 2010-04 /pmc/articles/PMC2931124/ /pubmed/20835327 http://dx.doi.org/10.4103/0971-4065.65306 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 Bahadur, M. M. Binnani, P. Gupta, R. Pattewar, S. Marginal donor kidney in a marginal recipient: Five year follow-up |
title | Marginal donor kidney in a marginal recipient: Five year follow-up |
title_full | Marginal donor kidney in a marginal recipient: Five year follow-up |
title_fullStr | Marginal donor kidney in a marginal recipient: Five year follow-up |
title_full_unstemmed | Marginal donor kidney in a marginal recipient: Five year follow-up |
title_short | Marginal donor kidney in a marginal recipient: Five year follow-up |
title_sort | marginal donor kidney in a marginal recipient: five year follow-up |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2931124/ https://www.ncbi.nlm.nih.gov/pubmed/20835327 http://dx.doi.org/10.4103/0971-4065.65306 |
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