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Renal manifestations of severe Rabson-Mendenhall syndrome: a case report

INTRODUCTION: Rabson-Mendenhall Syndrome (RMS) is a rare form of severe insulin resistance due to a recessive mutation of the insulin receptor. Associated manifestations include facial dysmorphism, skin abnormalities, and renal anomalies. CASE PRESENTATION: We report a case of a 13 year old African...

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Autores principales: Chong, Yih Harng, Taylor, Barry J, Wheeler, Benjamin J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598197/
https://www.ncbi.nlm.nih.gov/pubmed/23497647
http://dx.doi.org/10.1186/2251-6581-12-7
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author Chong, Yih Harng
Taylor, Barry J
Wheeler, Benjamin J
author_facet Chong, Yih Harng
Taylor, Barry J
Wheeler, Benjamin J
author_sort Chong, Yih Harng
collection PubMed
description INTRODUCTION: Rabson-Mendenhall Syndrome (RMS) is a rare form of severe insulin resistance due to a recessive mutation of the insulin receptor. Associated manifestations include facial dysmorphism, skin abnormalities, and renal anomalies. CASE PRESENTATION: We report a case of a 13 year old African female with RMS, severe insulin resistance, and a cluster of renal pathologies including nephromegaly, nephrolithiasis, hydronephrosis, and medullary sponge kidney. CONCLUSION: This is the first case of severe insulin resistance associated with the collection of renal conditions described. We postulate that renal conditions present in RMS may be under recognised, and recommend screening for the above conditions. This case adds to the scarce body of literature of associated renal manifestations with RMS, including medullary sponge kidney, across the spectrum of insulin resistance.
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spelling pubmed-35981972013-03-20 Renal manifestations of severe Rabson-Mendenhall syndrome: a case report Chong, Yih Harng Taylor, Barry J Wheeler, Benjamin J J Diabetes Metab Disord Case Report INTRODUCTION: Rabson-Mendenhall Syndrome (RMS) is a rare form of severe insulin resistance due to a recessive mutation of the insulin receptor. Associated manifestations include facial dysmorphism, skin abnormalities, and renal anomalies. CASE PRESENTATION: We report a case of a 13 year old African female with RMS, severe insulin resistance, and a cluster of renal pathologies including nephromegaly, nephrolithiasis, hydronephrosis, and medullary sponge kidney. CONCLUSION: This is the first case of severe insulin resistance associated with the collection of renal conditions described. We postulate that renal conditions present in RMS may be under recognised, and recommend screening for the above conditions. This case adds to the scarce body of literature of associated renal manifestations with RMS, including medullary sponge kidney, across the spectrum of insulin resistance. BioMed Central 2013-01-22 /pmc/articles/PMC3598197/ /pubmed/23497647 http://dx.doi.org/10.1186/2251-6581-12-7 Text en Copyright ©2013 Chong et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chong, Yih Harng
Taylor, Barry J
Wheeler, Benjamin J
Renal manifestations of severe Rabson-Mendenhall syndrome: a case report
title Renal manifestations of severe Rabson-Mendenhall syndrome: a case report
title_full Renal manifestations of severe Rabson-Mendenhall syndrome: a case report
title_fullStr Renal manifestations of severe Rabson-Mendenhall syndrome: a case report
title_full_unstemmed Renal manifestations of severe Rabson-Mendenhall syndrome: a case report
title_short Renal manifestations of severe Rabson-Mendenhall syndrome: a case report
title_sort renal manifestations of severe rabson-mendenhall syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598197/
https://www.ncbi.nlm.nih.gov/pubmed/23497647
http://dx.doi.org/10.1186/2251-6581-12-7
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