扩张型心肌病
桑格测序
外显子组测序
遗传学
医学遗传学
基因检测
移码突变
先证者
医学
基因组学
生物信息学
生物
基因
DNA测序
突变
内科学
基因组
心力衰竭
作者
Yanlong Ren,Yahui Zhang,Xiaoping Zhang,Yue-Li Wang,Xuxia Liu,Shengye Jin,Shangqiu Ning,Wenxian Liu,Xiaoyan Li
出处
期刊:PubMed
日期:2023-12-10
卷期号:40 (12): 1551-1555
标识
DOI:10.3760/cma.j.cn511374-20220606-00383
摘要
To explore the genetic basis for a patient with Dilated cardiomyopathy.A patient admitted to Beijing Anzhen Hospital Affiliated to Capital Medical University in April 2022 was selected as the study subject. Clinical data and family history of the patient was collected. Targeted exome sequencing was carried out. Candidate variant was verified by Sanger sequencing and bioinformatic analysis based on guidelines of the American College of Medical Genetics and Genomics (ACMG).DNA sequencing revealed that the patient has harbored a heterozygous c.5044dupG frameshift variant of the FLNC gene. Based on the ACMG guidelines, the variant was predicted to be likely pathogenic (PVS1+PM2_Supporting+PP4).The heterozygous c.5044dupG variant of the FLNC gene probably underlay the pathogenesis in this patient, which has provided a basis for the genetic counseling for his family.
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