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Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists
Because autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic abnormalities seen in today's medical practice, many internists will likely treat patients affected by this condition. Genetic abnormalities have been increasingly recognized, and the pathophysiology...
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Formato: | Texto |
Lenguaje: | English |
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The Korean Association of Internal Medicine
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732773/ https://www.ncbi.nlm.nih.gov/pubmed/19721850 http://dx.doi.org/10.3904/kjim.2009.24.3.165 |
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author | Bennett, William M. |
author_facet | Bennett, William M. |
author_sort | Bennett, William M. |
collection | PubMed |
description | Because autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic abnormalities seen in today's medical practice, many internists will likely treat patients affected by this condition. Genetic abnormalities have been increasingly recognized, and the pathophysiology of the disease is beginning to be unraveled. Because of advances in imaging technology, surrogate markers for disease progression have allowed clinical studies of newer therapeutic agents to proceed. In the near future, therapies for this common genetic disease may be available to either prevent or stabilize the disease course for many affected individuals. |
format | Text |
id | pubmed-2732773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Korean Association of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-27327732009-09-01 Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists Bennett, William M. Korean J Intern Med Review Because autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic abnormalities seen in today's medical practice, many internists will likely treat patients affected by this condition. Genetic abnormalities have been increasingly recognized, and the pathophysiology of the disease is beginning to be unraveled. Because of advances in imaging technology, surrogate markers for disease progression have allowed clinical studies of newer therapeutic agents to proceed. In the near future, therapies for this common genetic disease may be available to either prevent or stabilize the disease course for many affected individuals. The Korean Association of Internal Medicine 2009-09 2009-08-26 /pmc/articles/PMC2732773/ /pubmed/19721850 http://dx.doi.org/10.3904/kjim.2009.24.3.165 Text en Copyright © 2009 The Korean Association of Internal Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Bennett, William M. Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists |
title | Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists |
title_full | Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists |
title_fullStr | Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists |
title_full_unstemmed | Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists |
title_short | Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists |
title_sort | autosomal dominant polycystic kidney disease: 2009 update for internists |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732773/ https://www.ncbi.nlm.nih.gov/pubmed/19721850 http://dx.doi.org/10.3904/kjim.2009.24.3.165 |
work_keys_str_mv | AT bennettwilliamm autosomaldominantpolycystickidneydisease2009updateforinternists |