The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children
There is still no comprehensive description of the general population regarding clinical features and genetic etiology for co-occurring epilepsy and autism spectrum disorder (ASD) in Chinese children. This study was a retrospective study of children diagnosed with epilepsy and ASD from January 1st,...
Main Authors: | Shasha Long, Hao Zhou, Shuang Li, Tianqi Wang, Yu Ma, Chunpei Li, Yuanfeng Zhou, Shuizhen Zhou, Bingbing Wu, Yi Wang |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2019-05-01
|
Series: | Frontiers in Neurology |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fneur.2019.00505/full |
Similar Items
-
Application of Trio-Whole Exome Sequencing in Genetic Diagnosis and Therapy in Chinese Children With Epilepsy
by: Tiejia Jiang, et al.
Published: (2021-08-01) -
Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes
by: Ioannis Zaganas, et al.
Published: (2021-01-01) -
Intravenous Topiramate: Pharmacokinetics in Dogs with Naturally-Occurring Epilepsy
by: Irene Vuu, et al.
Published: (2016-12-01) -
Recurrent NUS1 canonical splice donor site mutation in two unrelated individuals with epilepsy, myoclonus, ataxia and scoliosis - a case report
by: Kouhei Den, et al.
Published: (2019-10-01) -
SYN1 Mutation Causes X-Linked Toothbrushing Epilepsy in a Chinese Family
by: Qin Zhou, et al.
Published: (2021-09-01)