Hebbar Malavika, Mefford Heather C
Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA, 98105, USA.
F1000Res. 2020 Mar 12;9. doi: 10.12688/f1000research.21366.1. eCollection 2020.
Developmental and epileptic encephalopathies (DEEs) are a group of severe, early onset epilepsies characterized by refractory seizures, developmental delay or regression associated with ongoing epileptic activity, and generally poor prognosis. DEE is genetically and phenotypically heterogeneous, and there is a plethora of genetic testing options to investigate the rapidly growing list of epilepsy genes. However, more than 50% of patients with DEE remain without a genetic diagnosis despite state-of-the-art genetic testing. In this review, we discuss the major advances in epilepsy genomics that have surfaced in recent years. The goal of this review is to reach a larger audience and build a better understanding of pathogenesis and genetic testing options in DEE.
发育性和癫痫性脑病(DEEs)是一组严重的早发性癫痫,其特征为难治性癫痫发作、与持续癫痫活动相关的发育迟缓或倒退,且预后通常较差。DEE在遗传和表型上具有异质性,有大量的基因检测选项可用于研究迅速增加的癫痫相关基因列表。然而,尽管采用了最先进的基因检测,仍有超过50%的DEE患者没有得到基因诊断。在本综述中,我们讨论了近年来癫痫基因组学方面出现的主要进展。本综述的目的是让更多人了解并更好地理解DEE的发病机制和基因检测选项。