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COQ8B-Related Steroid-Resistant Nephrotic Syndrome in Saudi Arabia: A Case Report

The CoQ10 enzyme has several vital roles in the human body. CoQ10 deficiency can lead to many clinical manifestations including the steroid-resistant nephrotic syndrome. At least 16 genes work together to facilitate the correct synthesis of CoQ10, one of which is CoQ8B. We report the case of a 14-ye...

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Autores principales: Alvi, Nasser H, Turkstani, Bakur A, Ashi, Ahmad S, Alzahrani, Abdullah M, Tawffeq, Abdulaziz M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749873/
https://www.ncbi.nlm.nih.gov/pubmed/36532926
http://dx.doi.org/10.7759/cureus.31922
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author Alvi, Nasser H
Turkstani, Bakur A
Ashi, Ahmad S
Alzahrani, Abdullah M
Tawffeq, Abdulaziz M
author_facet Alvi, Nasser H
Turkstani, Bakur A
Ashi, Ahmad S
Alzahrani, Abdullah M
Tawffeq, Abdulaziz M
author_sort Alvi, Nasser H
collection PubMed
description The CoQ10 enzyme has several vital roles in the human body. CoQ10 deficiency can lead to many clinical manifestations including the steroid-resistant nephrotic syndrome. At least 16 genes work together to facilitate the correct synthesis of CoQ10, one of which is CoQ8B. We report the case of a 14-year-old male with a rare homozygous variant, who presented with late severe nephrotic syndrome and bilateral small dysplastic kidneys. This report will also describe the comprehensive and systemic workup that is needed in these patients. We conclude that physicians need to consider renal causes in their workup of any unexplained oedema in children and that in such cases, screening for rarer genetic causes should be considered in a country such as Saudi Arabia, given the relatively high rates of consanguinity here.
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spelling pubmed-97498732022-12-15 COQ8B-Related Steroid-Resistant Nephrotic Syndrome in Saudi Arabia: A Case Report Alvi, Nasser H Turkstani, Bakur A Ashi, Ahmad S Alzahrani, Abdullah M Tawffeq, Abdulaziz M Cureus Genetics The CoQ10 enzyme has several vital roles in the human body. CoQ10 deficiency can lead to many clinical manifestations including the steroid-resistant nephrotic syndrome. At least 16 genes work together to facilitate the correct synthesis of CoQ10, one of which is CoQ8B. We report the case of a 14-year-old male with a rare homozygous variant, who presented with late severe nephrotic syndrome and bilateral small dysplastic kidneys. This report will also describe the comprehensive and systemic workup that is needed in these patients. We conclude that physicians need to consider renal causes in their workup of any unexplained oedema in children and that in such cases, screening for rarer genetic causes should be considered in a country such as Saudi Arabia, given the relatively high rates of consanguinity here. Cureus 2022-11-26 /pmc/articles/PMC9749873/ /pubmed/36532926 http://dx.doi.org/10.7759/cureus.31922 Text en Copyright © 2022, Alvi et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Genetics
Alvi, Nasser H
Turkstani, Bakur A
Ashi, Ahmad S
Alzahrani, Abdullah M
Tawffeq, Abdulaziz M
COQ8B-Related Steroid-Resistant Nephrotic Syndrome in Saudi Arabia: A Case Report
title COQ8B-Related Steroid-Resistant Nephrotic Syndrome in Saudi Arabia: A Case Report
title_full COQ8B-Related Steroid-Resistant Nephrotic Syndrome in Saudi Arabia: A Case Report
title_fullStr COQ8B-Related Steroid-Resistant Nephrotic Syndrome in Saudi Arabia: A Case Report
title_full_unstemmed COQ8B-Related Steroid-Resistant Nephrotic Syndrome in Saudi Arabia: A Case Report
title_short COQ8B-Related Steroid-Resistant Nephrotic Syndrome in Saudi Arabia: A Case Report
title_sort coq8b-related steroid-resistant nephrotic syndrome in saudi arabia: a case report
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749873/
https://www.ncbi.nlm.nih.gov/pubmed/36532926
http://dx.doi.org/10.7759/cureus.31922
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