Suppr超能文献

常染色体隐性遗传青少年综合征性肾单位肾痨由新型复合杂合致病性变异引起。

Autosomal Recessive Adolescent Syndromic Nephronophthisis Caused by a Novel Compound Heterozygous Pathogenic Variant.

机构信息

Department of Medicine, Renal Division, Emory University School of Medicine, Atlanta, GA, USA.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.

出版信息

Am J Case Rep. 2023 Nov 22;24:e941413. doi: 10.12659/AJCR.941413.

Abstract

BACKGROUND Nephronophthisis, an autosomal recessive ciliopathy involving mutations in primary cilium genes, is characterized by chronic tubulointerstitial nephritis and a defective urine concentrating capacity. It accounts for about 5% of renal failure in children and adolescents and usually progresses to end-stage renal disease before the age of 30 years. Nephronophthisis is associated with extrarenal manifestations, including retinitis pigmentosa in Senior-Loken syndrome (SLS), and liver fibrosis in 10-20% of cases. While some presenting patterns could be characteristic, patients may have atypical presentation, making diagnosis difficult. Tubulointerstitial fibrosis is the predominant feature on histology and as such, diagnosis depends mostly on genetic testing. Despite advances in renal genomics over the years with a better understanding of primary cilia and ciliary theory, about 40% of nephronophthisis cases go undiagnosed. As the underlying genetic etiologies are not fully understood, morphologic pathologic findings are non-specific, and treatment options are limited to dialysis and transplantation. CASE REPORT We describe a unique case of a patient with adolescent nephronophthisis who presented with advanced chronic kidney disease and severe pancytopenia, who progressed to end-stage renal disease at the age of 19, and was found to have syndromic nephronophthisis with compound heterozygous inheritance. CONCLUSIONS This report highlights the atypical presentation patterns that can be seen in syndromic nephronophthisis, the importance of genetic diagnosis when there is a high index of suspicion, and the need to further study genetic variants to better understand and diagnose the disease and to develop targeted therapy.

摘要

背景

常染色体隐性遗传纤毛病,涉及初级纤毛基因的突变,其特征为慢性肾小管间质性肾炎和尿浓缩功能缺陷。它约占儿童和青少年肾衰竭的 5%,通常在 30 岁之前进展为终末期肾病。纤毛病与肾脏外表现有关,包括 Senior-Loken 综合征(SLS)的视网膜色素变性,以及 10-20%病例的肝纤维化。虽然某些表现形式可能具有特征性,但患者可能表现出非典型症状,导致诊断困难。组织学上以肾小管间质性纤维化为主,因此,诊断主要依赖于基因检测。尽管近年来在肾脏基因组学方面取得了进展,对初级纤毛和纤毛理论有了更好的理解,但仍有 40%的纤毛病病例未得到诊断。由于尚未完全了解潜在的遗传病因,形态病理发现是非特异性的,治疗选择仅限于透析和移植。病例报告:我们描述了一例青少年纤毛病患者的独特病例,该患者表现为晚期慢性肾脏病和严重全血细胞减少症,19 岁时进展为终末期肾病,并被发现患有综合征性纤毛病,具有复合杂合遗传。结论:本报告强调了综合征性纤毛病可能出现的非典型表现模式,当高度怀疑时进行基因诊断的重要性,以及进一步研究遗传变异以更好地理解和诊断疾病并开发靶向治疗的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f0/10681955/b7cb1f6aeff1/amjcaserep-24-e941413-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验