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Survival over 2 years of autosomal-recessive renal tubular dysgenesis
Autosomal-recessive renal tubular dysgenesis (AR-RTD) is a rare disorder caused by a genetic defect in the renin–angiotensin system. Although AR-RTD has typically been known as a lethal disease due to refractory hypotension and renal failure immediately after birth, few cases have reported survival...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400456/ https://www.ncbi.nlm.nih.gov/pubmed/26069751 http://dx.doi.org/10.1093/ndtplus/sfr153 |
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author | Kim, Su Yeong Kang, Hee Gyung Kim, Ee Kyung Choi, Jung Hwan Choi, Yong Cheong, Hae Il |
author_facet | Kim, Su Yeong Kang, Hee Gyung Kim, Ee Kyung Choi, Jung Hwan Choi, Yong Cheong, Hae Il |
author_sort | Kim, Su Yeong |
collection | PubMed |
description | Autosomal-recessive renal tubular dysgenesis (AR-RTD) is a rare disorder caused by a genetic defect in the renin–angiotensin system. Although AR-RTD has typically been known as a lethal disease due to refractory hypotension and renal failure immediately after birth, few cases have reported survival of the neonatal period. We report here an additional case of AR-RTD, who had novel ACE mutations and survived over 2 years and provide a review of the five previously reported surviving cases. In conclusion, AR-RTD is not a uniformly fatal disease, although factors affecting the survival remain unknown. |
format | Online Article Text |
id | pubmed-4400456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44004562015-06-11 Survival over 2 years of autosomal-recessive renal tubular dysgenesis Kim, Su Yeong Kang, Hee Gyung Kim, Ee Kyung Choi, Jung Hwan Choi, Yong Cheong, Hae Il Clin Kidney J Clinical Cases Autosomal-recessive renal tubular dysgenesis (AR-RTD) is a rare disorder caused by a genetic defect in the renin–angiotensin system. Although AR-RTD has typically been known as a lethal disease due to refractory hypotension and renal failure immediately after birth, few cases have reported survival of the neonatal period. We report here an additional case of AR-RTD, who had novel ACE mutations and survived over 2 years and provide a review of the five previously reported surviving cases. In conclusion, AR-RTD is not a uniformly fatal disease, although factors affecting the survival remain unknown. Oxford University Press 2012-02 2012-01-28 /pmc/articles/PMC4400456/ /pubmed/26069751 http://dx.doi.org/10.1093/ndtplus/sfr153 Text en © The Author 2012. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com http://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 (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Clinical Cases Kim, Su Yeong Kang, Hee Gyung Kim, Ee Kyung Choi, Jung Hwan Choi, Yong Cheong, Hae Il Survival over 2 years of autosomal-recessive renal tubular dysgenesis |
title | Survival over 2 years of autosomal-recessive renal tubular dysgenesis |
title_full | Survival over 2 years of autosomal-recessive renal tubular dysgenesis |
title_fullStr | Survival over 2 years of autosomal-recessive renal tubular dysgenesis |
title_full_unstemmed | Survival over 2 years of autosomal-recessive renal tubular dysgenesis |
title_short | Survival over 2 years of autosomal-recessive renal tubular dysgenesis |
title_sort | survival over 2 years of autosomal-recessive renal tubular dysgenesis |
topic | Clinical Cases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400456/ https://www.ncbi.nlm.nih.gov/pubmed/26069751 http://dx.doi.org/10.1093/ndtplus/sfr153 |
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