• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

扩展肾单位-纤毛相关疾病表型:一名携带 RPGRIP1L 纯合突变的老年患者。

Expanding Phenotype of Nephronophthisis-Related Ciliopathy: an Elderly Patient with Homozygous RPGRIP1L Mutation.

机构信息

Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.

Apheresis and Dialysis Center, School of Medicine, Keio University, Tokyo, Japan.

出版信息

Nephron. 2018;140(1):74-78. doi: 10.1159/000490770. Epub 2018 Jul 10.

DOI:10.1159/000490770
PMID:29991045
Abstract

Nephronophthisis-related ciliopathies (NPHP-RC) are autosomal recessive disorders characterized by renal corticomedullary cysts with the extrarenal symptoms. Typically, patients with NPHP-RC reach end-stage kidney disease (ESKD) before the age of 30 years. We herein report a Japanese woman with NPHP-RC who had unusually delayed progression to ESKD after 6 decades. She exhibited liver dysfunction at the age of 23 years. She also showed mild renal dysfunction at the age of 43 years. Ultrasonography revealed bilateral multiple renal cysts with loss of corticomedullary differentiation. Her liver and renal functions gradually deteriorated. She was diagnosed with liver fibrosis as a result of biopsy, and initiated the maintenance hemodiafiltration therapy for ESKD at the age of 61 years. Because of a unique combination of multiple renal cysts and liver fibrosis, ciliopathy was suspected and medical exome analysis was performed. A novel homozygous missense mutation was identified in RPGRIP1L (c.1810G>A p.Glu604Lys), a causative gene for NPHP-RC. To the best of our knowledge, this patient is the oldest one who progressed to ESKD in NPHP-RC. Our case illustrates that NPHP-RC should be included in the differential diagnosis of the patient with corticomedullary polycystic kidneys accompanied by the extrarenal organ involvements, even if the patient is elderly.

摘要

肾单位肾痨相关纤毛病(NPHP-RC)是一种常染色体隐性遗传病,其特征为肾皮质髓质囊肿伴肾外症状。通常,NPHP-RC 患者在 30 岁之前就会进展到终末期肾病(ESKD)。本文报告了一例日本女性 NPHP-RC 患者,她在 60 多岁后才出现异常的 ESKD 进展延迟。她在 23 岁时出现肝功能异常,43 岁时出现轻度肾功能异常。超声检查显示双侧多发性肾囊肿,皮质髓质分化丧失。她的肝功能和肾功能逐渐恶化。由于肝活检结果为肝纤维化,她开始进行 ESKD 的维持性血液透析滤过治疗。由于多种肾囊肿和肝纤维化的独特组合,怀疑存在纤毛病,并进行了医学外显子组分析。在 NPHP-RC 的致病基因 RPGRIP1L 中发现了一个新的纯合错义突变(c.1810G>A p.Glu604Lys)。据我们所知,该患者是 NPHP-RC 中进展到 ESKD 年龄最大的患者。本病例说明,即使患者年龄较大,对于伴有肾外器官受累的皮质髓质多囊肾病患者,也应将 NPHP-RC 纳入鉴别诊断。

相似文献

1
Expanding Phenotype of Nephronophthisis-Related Ciliopathy: an Elderly Patient with Homozygous RPGRIP1L Mutation.扩展肾单位-纤毛相关疾病表型:一名携带 RPGRIP1L 纯合突变的老年患者。
Nephron. 2018;140(1):74-78. doi: 10.1159/000490770. Epub 2018 Jul 10.
2
Mutations of ADAMTS9 Cause Nephronophthisis-Related Ciliopathy.ADAMTS9 基因突变导致与肾单位纤毛病相关的纤毛病。
Am J Hum Genet. 2019 Jan 3;104(1):45-54. doi: 10.1016/j.ajhg.2018.11.003.
3
Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis-related ciliopathy.靶向外显子组测序解决了肾单位肾痨相关纤毛病基因诊断中的等位基因和基因异质性问题。
Exp Mol Med. 2016 Aug 5;48(8):e251. doi: 10.1038/emm.2016.63.
4
Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy.荷兰 40 例肾单位肾痨相关纤毛病患者的临床和遗传学分析。
Pediatr Nephrol. 2018 Oct;33(10):1701-1712. doi: 10.1007/s00467-018-3958-7. Epub 2018 Jul 5.
5
Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies.肾单位肾痨病及相关纤毛病患儿的表型谱。
Clin J Am Soc Nephrol. 2017 Dec 7;12(12):1974-1983. doi: 10.2215/CJN.01280217. Epub 2017 Nov 16.
6
Genotype and phenotype analysis and transplantation strategy in children with kidney failure caused by NPHP.基因型和表型分析及在 NPHP 导致的肾衰竭患儿中的移植策略。
Pediatr Nephrol. 2023 May;38(5):1609-1620. doi: 10.1007/s00467-022-05763-3. Epub 2022 Oct 13.
7
Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencing.通过靶向重测序在非近亲家庭中鉴定出的罕见肾纤毛病。
Clin Exp Nephrol. 2017 Feb;21(1):136-142. doi: 10.1007/s10157-016-1256-x. Epub 2016 Mar 11.
8
Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathy.中国肾单位-集合管相关纤毛病患者的表型和基因型谱。
J Med Genet. 2022 Feb;59(2):147-154. doi: 10.1136/jmedgenet-2020-107184. Epub 2020 Dec 15.
9
Nephronophthisis and related syndromes.肾痨及相关综合征。
Curr Opin Pediatr. 2015 Apr;27(2):201-11. doi: 10.1097/MOP.0000000000000194.
10
Rapidly Progressive Nephronophthisis in a 2-Year-Old Boy with a Homozygous SDCCAG8 Mutation.2 岁男孩患快速进展性肾单位肾痨,携带 SDCCAG8 纯合突变。
Tohoku J Exp Med. 2019 Sep;249(1):29-32. doi: 10.1620/tjem.249.29.