类固醇抵抗性肾病综合征患儿肾小球基底膜息肉样改变及ARHGAP24突变1例

A. Francis, J. Burke, L. Francis, S. McTaggart, A. Mallett
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引用次数: 1

摘要

背景:随着足细胞和基底膜蛋白编码基因的大量突变的发现,类固醇抵抗性肾病综合征(SRNS)越来越被认为具有遗传基础。ARHGAP24基因产物最近被认为是足细胞与肾小球基底膜相互作用的重要参与者。ARHGAP24基因编码一种参与调节细胞运动、膜结构和极性的蛋白质。该基因的突变在体外已被证明会引起细胞膜褶皱。病例介绍:我们报告了一个新的外显子4错义突变(c.[284G> a];p.[Arg95Gln])在4岁时表现为SRNS的儿童中ARHGAP24基因的表达。肾活检显示肾小球基底膜(GBM)异常息肉样改变。结论:我们认为这种新的ARHGAP24突变是SRNS与异常息肉基底膜改变相关的病因。这些与ARHGAP24突变和临床肾病综合征相关的活检结果是一个新发现。这一发现可能促进对ARHGAP24基因产物功能的认识。
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Polypoid Change of the Glomerular Basement Membrane in a Child with Steroid Resistant Nephrotic Syndrome and ARHGAP24 Mutation: A Case Report
Background: Steroid resistant nephrotic syndrome (SRNS) is increasingly recognised to have a genetic basis following the identification of a number of mutations within genes encoding podocyte and basement membrane proteins. The ARHGAP24 gene product is a recently recognised important player in podocyte interaction with the glomerular basement membrane. The ARHGAP24 gene encodes a protein involved in regulating cell motility, membrane structure and polarity. Mutations in the gene have been showin vitro to cause cell membrane ruffling. Case Presentation: We report a novel missense mutation in exon 4 (c.[284G>A]; p.[Arg95Gln]) of the ARHGAP24 gene in a child that presented with SRNS at four years of age. Renal biopsy demonstrated unusual polypoid changes of the glomerular basement membrane (GBM). Conclusion: We propose this novel ARHGAP24 mutation as causative for SRNS associated with unusual polypoid basement membrane changes. These biopsy findings, in association with ARHGAP24 mutation and clinical nephrotic syndrome are a novel finding. This finding may advance the understanding of ARHGAP24 gene product function.
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