Clinical phenotype features and genetic etiologies of 38 children with progressive myoclonic epilepsy

Clinical phenotype features and genetic etiologies of 38 children with progressive myoclonic epilepsy

Abstract Background Progressive myoclonic epilepsy (PME) is a group of neurodegenerative diseases with genetic heterogeneity and phenotypic similarities, and many cases remain unknown of the genetic causes. This study is aim to summarize the clinical features and study the genetic causes of PME pati...

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Bibliographic Details
Main Authors: Jing Zhang, Ying Yang, Xueyang Niu, Jiaoyang Chen, Wei Sun, Changhong Ding, Lifang Dai, Liping Zhang, Qi Zeng, Yi Chen, Xiaojuan Tian, Xiaoling Yang, Taoyun Ji, Zhixian Yang, Yanling Yang, Yuwu Jiang, Yuehua Zhang
Format: Article
Language:English
Published: BMC 2020-09-01
Series:Acta Epileptologica
Subjects:
Progressive myoclonic epilepsy
Genotype
Phenotype
Online Access:http://link.springer.com/article/10.1186/s42494-020-00023-z

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http://link.springer.com/article/10.1186/s42494-020-00023-z

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