Survival over 2 years of autosomal-recessive renal tubular dysgenesis

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Abstract

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. © 2012 The Author 2012. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.

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Kim, S. Y., Kang, H. G., Kim, E. K., Choi, J. H., Choi, Y., & Cheong, H. I. (2012). Survival over 2 years of autosomal-recessive renal tubular dysgenesis. Clinical Kidney Journal, 5(1), 56–58. https://doi.org/10.1093/ndtplus/sfr153

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