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Schimke Immuno-osseous Dysplasia: A Case Report
Schimke immuno-osseous dysplasia (SIOD) is a rare inherited disease characterized by steroid resistant nephrotic syndrome, spondyloepiphyseal dysplasia, and T-cell immunodeficiency. Focal segmental glomerulosclerosis (FSGS) is the most frequent renal pathological finding associated with proteinuria...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668313/ https://www.ncbi.nlm.nih.gov/pubmed/31423066 http://dx.doi.org/10.4103/ijn.IJN_95_18 |
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author | Babaei, Amir Hossein Inaloo, Soroor Basiratnia, Mitra |
author_facet | Babaei, Amir Hossein Inaloo, Soroor Basiratnia, Mitra |
author_sort | Babaei, Amir Hossein |
collection | PubMed |
description | Schimke immuno-osseous dysplasia (SIOD) is a rare inherited disease characterized by steroid resistant nephrotic syndrome, spondyloepiphyseal dysplasia, and T-cell immunodeficiency. Focal segmental glomerulosclerosis (FSGS) is the most frequent renal pathological finding associated with proteinuria in SIOD. In this case report, we describe a 4.5-year-old boy who presented with nephrotic syndrome and ventricular septal defect followed by tremor in the limbs after-cerebral infarction. It is emphasized that SIOD should be considered in children with wide range of presentation, from growth retardation, steroid resistant nephrotic syndrome, and bone, cardiac, and neurological abnormalities in the late childhood or even adolescence. |
format | Online Article Text |
id | pubmed-6668313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-66683132019-08-16 Schimke Immuno-osseous Dysplasia: A Case Report Babaei, Amir Hossein Inaloo, Soroor Basiratnia, Mitra Indian J Nephrol Case Report Schimke immuno-osseous dysplasia (SIOD) is a rare inherited disease characterized by steroid resistant nephrotic syndrome, spondyloepiphyseal dysplasia, and T-cell immunodeficiency. Focal segmental glomerulosclerosis (FSGS) is the most frequent renal pathological finding associated with proteinuria in SIOD. In this case report, we describe a 4.5-year-old boy who presented with nephrotic syndrome and ventricular septal defect followed by tremor in the limbs after-cerebral infarction. It is emphasized that SIOD should be considered in children with wide range of presentation, from growth retardation, steroid resistant nephrotic syndrome, and bone, cardiac, and neurological abnormalities in the late childhood or even adolescence. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6668313/ /pubmed/31423066 http://dx.doi.org/10.4103/ijn.IJN_95_18 Text en Copyright: © 2019 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 Babaei, Amir Hossein Inaloo, Soroor Basiratnia, Mitra Schimke Immuno-osseous Dysplasia: A Case Report |
title | Schimke Immuno-osseous Dysplasia: A Case Report |
title_full | Schimke Immuno-osseous Dysplasia: A Case Report |
title_fullStr | Schimke Immuno-osseous Dysplasia: A Case Report |
title_full_unstemmed | Schimke Immuno-osseous Dysplasia: A Case Report |
title_short | Schimke Immuno-osseous Dysplasia: A Case Report |
title_sort | schimke immuno-osseous dysplasia: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668313/ https://www.ncbi.nlm.nih.gov/pubmed/31423066 http://dx.doi.org/10.4103/ijn.IJN_95_18 |
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