临床儿科杂志 ›› 2020, Vol. 38 ›› Issue (2): 101-.doi: 10.3969/j.issn.1000-3606.2020.02.006

• 泌尿系统疾病专栏 • 上一篇    下一篇

儿童Alport 综合征1 例COL4A5 基因新发突变分析

贾实磊, 高晓洁, 马颐姣, 刘俐兵, 倪芬芬, 李俊   

  1. 深圳市儿童医院肾脏科(广东深圳 518026)
  • 发布日期:2020-02-20
  • 通讯作者: 高晓洁 电子信箱:gxj0824@hotmail.com

Analysis of a novel mutation of COL4A5 gene in a child with Alport syndrome

 JIA Shilei, GAO Xiaojie, MA Yijiao, LIU Libing, NI Fenfen, LI Jun   

  1. Department of Nephrology, Shenzhen Children’s Hospital, Shenzhen 518038, Guangdong, China
  • Published:2020-02-20

摘要:  目的 分析儿童Alport综合征的基因型和临床特点。方法 回顾分析1例Alport综合征患儿的临床资料及 基因检测结果。结果 患儿男性,11岁, 7岁出现不明原因的血尿、蛋白尿,肾功能轻度异常,因治疗依从性差而进展至慢 性肾脏病尿毒症期。肾穿刺活检病理显示,慢性硬化性肾小球病变,弥漫性肾小管萎缩(萎缩面积超80%);免疫荧光染 色α3、α 5(IV)基底膜染色阳性。基因检测显示,COL4A5基因存在的一处半合子突变c.2631dupA(插入突变),导致氨 基酸改变p.G878Rfs*20(移码突变20位后蛋白翻译提前终止);家系验证其为新发突变,父母均未携带。依据ACMG指 南,该突变变异类型为致病性突变。查阅HGMDpro数据库未见报道。结论 基因检测有助于确诊Alport综合征,新发现 COL4A5基因半合子突变。

关键词: 基因突变; COL4A5; Aport综合征

Abstract: Objective To analyze the genotype and clinical characteristics of Alport syndrome in children. Methods Clinical manifestation and genetic test results of 1 Chinese boy with Alport syndrome were retrospectively analyzed. Results The 11-year-old male patient presented with unexplained hematuria and proteinuria with mild renal dysfunction 4 years ago and progressed to the uremia stage of chronic kidney disease due to poor treatment compliance. There was no high-frequency hearing impairment and ocular fundus pathology. Renal biopsy showed chronic sclerosing glomerular disease and diffuse tubular atrophy (atrophy area over 80%). Immunofluorescence staining of basement membrane of alpha 3 and alpha 5 (IV) were positive. Gene sequencing identified a hemizygous mutation of c.2631dupA (insertion) in COL4A5 gene, resulted in amino acid changes of p.G878Rfs*20 (prematurely termination of protein translation after 20 amino acids). It was identified as a de novo mutation. According to ACMG guidelines. This variant is classified as pathogenic. It has not been reported in the HGMDpro database. Conclusion Gene sequencing is helpful for the diagnosis of Alport syndrome and the discovery of novel variant of COL4A5 gene.

Key words: genetic mutation; COL4A5; Alport syndrome