Clinical characteristics and genetic analysis of early epileptic encephalopathy caused by YWHAG gene mutation
10.3760/cma.j.cn113694-20200527-00393
- VernacularTitle:YWHAG基因突变致早发性癫痫性脑病临床特征与遗传学分析
- Author:
Daoqi MEI
;
Shiyue MEI
;
Yuan WANG
;
Zhihui TANG
;
Xiaoyi CHEN
;
Guohong CHEN
;
Yaodong ZHANG
;
Xiaona WANG
- From:
Chinese Journal of Neurology
2021;54(1):16-21
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To report a rare case of early onset epileptic encephalopathy caused by YWHAG gene mutation, and discuss the clinical and genetic characteristics as well as the diagnosis, treatment and prognosis of the disease.Methods:Clinical data of the patient with YWHAG gene deficiency from Department of Neurology, Children′s Hospital Affiliated to Zhengzhou University were collected in January 2018. The whole exome sequencing was performed on the core members of the family, and the characteristics of gene mutations were analyzed.Results:The proband is a girl, three years and 10 months old, presented to the outpatient department of neurology with a history of six-month intermittent convulsions, manifested as epilepsy seizures, mental retardation, motor delay and gait instability, ataxia. The brain magnetic resonance imaging showed myelinated dysplasia, and long-term video electroencephalogram (EEG) showed extensive 1.5-3.0 Hz slow spikes, and multiple spikes during sleep. During the monitoring, the children had clinical seizures and abnormal EEG discharges, indicating that myoclonus was accompanied by atypical absence of consciousness. Whole exome sequencing on the proband detected a de novo mutation c.169C>T (p.Arg57Cys) in YWHAG gene. According to American College of Medical Genetics guidelines (2015), the mutation was considered potentially pathogenic.Conclusion:Early epileptic encephalopathy caused by YWHAG gene mutation is very rare, and the variation of YWHAG gene c.169C>T is the possible pathogenic variation of the genetic cause of early onset epileptic encephalopathy in the proband.
