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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...

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Autores principales: Kim, Su Yeong, Kang, Hee Gyung, Kim, Ee Kyung, Choi, Jung Hwan, Choi, Yong, Cheong, Hae Il
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
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.
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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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