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A Case Report and Literature Review of Oligomeganephronia

A 23-year-old woman was admitted to the hospital with proteinuria and mildly elevated creatinine, and a renal biopsy confirmed the diagnosis of oligomeganephronia (OMN). OMN is an extremely rare bilateral renal hypoplastic disease, and its diagnosis mainly relies on the pathological results obtained...

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Autores principales: Wang, Xu-Hao, Pan, Lei, He, Shan, Kong, De-Lei, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980273/
https://www.ncbi.nlm.nih.gov/pubmed/35391889
http://dx.doi.org/10.3389/fmed.2022.811992
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author Wang, Xu-Hao
Pan, Lei
He, Shan
Kong, De-Lei
Wang, Wei
author_facet Wang, Xu-Hao
Pan, Lei
He, Shan
Kong, De-Lei
Wang, Wei
author_sort Wang, Xu-Hao
collection PubMed
description A 23-year-old woman was admitted to the hospital with proteinuria and mildly elevated creatinine, and a renal biopsy confirmed the diagnosis of oligomeganephronia (OMN). OMN is an extremely rare bilateral renal hypoplastic disease, and its diagnosis mainly relies on the pathological results obtained from renal biopsy. At present, there is no effective treatment for OMN. Here, we report a case with mild renal insufficiency and proteinuria as the main symptom and present a summary of the clinical characteristics of ON along with a review of the literature on OMN.
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spelling pubmed-89802732022-04-06 A Case Report and Literature Review of Oligomeganephronia Wang, Xu-Hao Pan, Lei He, Shan Kong, De-Lei Wang, Wei Front Med (Lausanne) Medicine A 23-year-old woman was admitted to the hospital with proteinuria and mildly elevated creatinine, and a renal biopsy confirmed the diagnosis of oligomeganephronia (OMN). OMN is an extremely rare bilateral renal hypoplastic disease, and its diagnosis mainly relies on the pathological results obtained from renal biopsy. At present, there is no effective treatment for OMN. Here, we report a case with mild renal insufficiency and proteinuria as the main symptom and present a summary of the clinical characteristics of ON along with a review of the literature on OMN. Frontiers Media S.A. 2022-03-22 /pmc/articles/PMC8980273/ /pubmed/35391889 http://dx.doi.org/10.3389/fmed.2022.811992 Text en Copyright © 2022 Wang, Pan, He, Kong and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Wang, Xu-Hao
Pan, Lei
He, Shan
Kong, De-Lei
Wang, Wei
A Case Report and Literature Review of Oligomeganephronia
title A Case Report and Literature Review of Oligomeganephronia
title_full A Case Report and Literature Review of Oligomeganephronia
title_fullStr A Case Report and Literature Review of Oligomeganephronia
title_full_unstemmed A Case Report and Literature Review of Oligomeganephronia
title_short A Case Report and Literature Review of Oligomeganephronia
title_sort case report and literature review of oligomeganephronia
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980273/
https://www.ncbi.nlm.nih.gov/pubmed/35391889
http://dx.doi.org/10.3389/fmed.2022.811992
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