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Recent advances in the clinical management of autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic systemic disorder causing the development of renal and hepatic cysts and decline in renal function. It affects around 1 in 1,000 live births. Early hypertension and progressive renal failure due to massive enlargement of cysts and fib...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000 Research Limited
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352922/ https://www.ncbi.nlm.nih.gov/pubmed/30755792 http://dx.doi.org/10.12688/f1000research.17109.1 |
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author | Torra, Roser |
author_facet | Torra, Roser |
author_sort | Torra, Roser |
collection | PubMed |
description | Autosomal dominant polycystic kidney disease (ADPKD) is a genetic systemic disorder causing the development of renal and hepatic cysts and decline in renal function. It affects around 1 in 1,000 live births. Early hypertension and progressive renal failure due to massive enlargement of cysts and fibrosis are hallmarks of the disease. This article reviews recent advances in ADPKD and focuses mainly on diagnosis, management, and prediction of the course of the disease. |
format | Online Article Text |
id | pubmed-6352922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-63529222019-02-11 Recent advances in the clinical management of autosomal dominant polycystic kidney disease Torra, Roser F1000Res Review Autosomal dominant polycystic kidney disease (ADPKD) is a genetic systemic disorder causing the development of renal and hepatic cysts and decline in renal function. It affects around 1 in 1,000 live births. Early hypertension and progressive renal failure due to massive enlargement of cysts and fibrosis are hallmarks of the disease. This article reviews recent advances in ADPKD and focuses mainly on diagnosis, management, and prediction of the course of the disease. F1000 Research Limited 2019-01-29 /pmc/articles/PMC6352922/ /pubmed/30755792 http://dx.doi.org/10.12688/f1000research.17109.1 Text en Copyright: © 2019 Torra R http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Torra, Roser Recent advances in the clinical management of autosomal dominant polycystic kidney disease |
title | Recent advances in the clinical management of autosomal dominant polycystic kidney disease |
title_full | Recent advances in the clinical management of autosomal dominant polycystic kidney disease |
title_fullStr | Recent advances in the clinical management of autosomal dominant polycystic kidney disease |
title_full_unstemmed | Recent advances in the clinical management of autosomal dominant polycystic kidney disease |
title_short | Recent advances in the clinical management of autosomal dominant polycystic kidney disease |
title_sort | recent advances in the clinical management of autosomal dominant polycystic kidney disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352922/ https://www.ncbi.nlm.nih.gov/pubmed/30755792 http://dx.doi.org/10.12688/f1000research.17109.1 |
work_keys_str_mv | AT torraroser recentadvancesintheclinicalmanagementofautosomaldominantpolycystickidneydisease |