摘要
2022390 Clinical characteristics and literature review of a case of Christianson syndrome caused by SLC9A6 gene variation.LI Xian(李娴),et al.Children's Hosp,Zhengzhou Univ,Henan Key Lab,Children's Genetic&Metab Dis,Zhengzhou 450018.Chin J Neurol 2022;55(8):834-841.Objective To retrospectively analyze the elinical data of Christianson syndrome caused by SLC9A6 gene mutation and the related literatures.Methods The clinical data of one Christianson syndrome patient caused by SLC9A6 gene variation in Children's Hospital of Zhengzhou University were collected,meanwhile the relevant literature was reviewed.The examination of video electroencephalogram,auditory brainstem response,and cranial magnetic resonance imaging(MRI)was.performed.
