医学
外显子组测序
家族史
队列
脑瘫
回顾性队列研究
拷贝数变化
基因检测
儿科
队列研究
生物信息学
内科学
遗传学
基因
突变
生物
物理疗法
基因组
作者
Hongfang Mei,Lin Yang,Xiaowen Tian,Sujuan Wang,Bingbing Wu,Huijun Wang,Yulan Lu,Xinran Dong,Hong Yuan,Wenhao Zhou
标识
DOI:10.1016/j.jpeds.2021.11.019
摘要
To explore the genetic spectrum of cerebral palsy (CP) in a Chinese pediatric cohort.This was a retrospective observational study of patients with CP from the Children's Hospital of Fudan University between June 2015 and December 2019. Their clinical data and exome sequencing data were collected and analyzed.A total of 217 patients with CP were enrolled, and genetic variants were identified in 78 subjects (35.9%): 65 patients with single-nucleotide variants (SNVs), 12 patients with copy number variants, and 1 patient with both an SNV and a copy number variant. The genetic diagnosis rates were significantly greater in patients without clinical risk factors than in patients with clinical risk factors (χ2 = 21.705, P = .000) and were significantly greater in patients with a family history than in those without a family history (χ2 = 4.493, P = .034). Variants in genes related to neurologic disorders were the most commonly detected variants, affecting 41 patients (62.1%, 41/66). Among the patients with SNVs detected, the top 12 genes were found to cover 62.1% (41/66) of cases, and 39.4% (26/66) of patients with SNVs had medically actionable genetic findings.The overall genetic diagnostic rate in this study was 35.9%, and patients without any clinical risk factors or with a family history were more likely to have genetic risk factors. The top 12 genes detected in this study as well as genes related to neurologic disorders or other medically actionable disorders should be noted in the analysis of genetic testing results in patients with CP.
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