Rare Association of Waardenburg Syndrome with Minimal Change Disease

Waardenburg syndrome (WS) is a rare genetic disorder characterized by varying degrees of hearing loss, pigmentary anomalies, and defects of other neural crest cell-derived structures. The association of WS with renal anomalies has been described in the literature. However, nephrotic syndrome is a ve...

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Autores principales: Anvesh, G., Raju, S. B., Prasad, K., Sharma, A., Surendra, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998718/
https://www.ncbi.nlm.nih.gov/pubmed/29962674
http://dx.doi.org/10.4103/ijn.IJN_55_17
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author Anvesh, G.
Raju, S. B.
Prasad, K.
Sharma, A.
Surendra, M.
author_facet Anvesh, G.
Raju, S. B.
Prasad, K.
Sharma, A.
Surendra, M.
author_sort Anvesh, G.
collection PubMed
description Waardenburg syndrome (WS) is a rare genetic disorder characterized by varying degrees of hearing loss, pigmentary anomalies, and defects of other neural crest cell-derived structures. The association of WS with renal anomalies has been described in the literature. However, nephrotic syndrome is a very rare association with WS, and only one case has been reported in the literature. We report a case of WS2 associated with biopsy-proven nephrotic syndrome (minimal change disease).
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spelling pubmed-59987182018-06-29 Rare Association of Waardenburg Syndrome with Minimal Change Disease Anvesh, G. Raju, S. B. Prasad, K. Sharma, A. Surendra, M. Indian J Nephrol Case Report Waardenburg syndrome (WS) is a rare genetic disorder characterized by varying degrees of hearing loss, pigmentary anomalies, and defects of other neural crest cell-derived structures. The association of WS with renal anomalies has been described in the literature. However, nephrotic syndrome is a very rare association with WS, and only one case has been reported in the literature. We report a case of WS2 associated with biopsy-proven nephrotic syndrome (minimal change disease). Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5998718/ /pubmed/29962674 http://dx.doi.org/10.4103/ijn.IJN_55_17 Text en Copyright: © 2018 Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Anvesh, G.
Raju, S. B.
Prasad, K.
Sharma, A.
Surendra, M.
Rare Association of Waardenburg Syndrome with Minimal Change Disease
title Rare Association of Waardenburg Syndrome with Minimal Change Disease
title_full Rare Association of Waardenburg Syndrome with Minimal Change Disease
title_fullStr Rare Association of Waardenburg Syndrome with Minimal Change Disease
title_full_unstemmed Rare Association of Waardenburg Syndrome with Minimal Change Disease
title_short Rare Association of Waardenburg Syndrome with Minimal Change Disease
title_sort rare association of waardenburg syndrome with minimal change disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998718/
https://www.ncbi.nlm.nih.gov/pubmed/29962674
http://dx.doi.org/10.4103/ijn.IJN_55_17
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