Ontology highlight
ABSTRACT:
SUBMITTER: Duan J
PROVIDER: S-EPMC9096209 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature
Duan Jing J Chen Yan Y Hu Zhanqi Z Ye Yuanzhen Y Zhang Tian T Li Cong C Zeng Qi Q Zhao Xia X Mai Jiahui J Sun Yang Y Liu Chao C Zheng Wenxin W Xiao Yuhan Y Liao Jianxiang J Chen Li L
Frontiers in pediatrics 20220428
Progressive myoclonic epilepsy (PME) is a group of rare diseases characterized by progressive myoclonus, cognitive impairment, ataxia, and other neurologic deficits. PME has high genetic heterogeneity, and more than 40 genes are reportedly associated with this disorder. <i>SEMA6B</i> encodes a member of the semaphorin family and was first reported to cause PME in 2020. Herein, we present a rare case of PME due to a novel <i>SEMA6B</i> gene mutation in a 6-year-old boy born to healthy non-consang ...[more]