Research Progress on Precise Diagnosis and Treatment of Developmental and Epileptic Encephalopathies

发育性癫痫性脑病(developmental and epilepsy encephalopathies, DEEs)是指起病于发育期,以精神运动发育迟缓或倒退为特征的一组癫痫性脑病综合征。DEEs病因及致病机制复杂,遗传因素占据主导地位。当前,病因驱动治疗已成为制定DEEs管理方案的核心,个别综合征亦有特定的药物适应症。本文综述了目前DEEs的遗传学病因及新型抗癫痫药物在DEEs中的应用前景。旨在优化治疗方案,强调个体化精准诊疗,为提高对这一罕见癫痫疾病的理解和管理提供理论支持。Developmental and epileptic encephalopathy (DEEs) refers to a group of epileptic encephalopathy syndromes that begin in the developmental period and are characterized by development delay or regression. The etiology and pathogenesis of DEEs are complex, with genetic factors dominating. Currently, etiology-driven treatment has become the core of DEEs management, and certain syndromes also have specific drug indications. This article reviews the current genetic etiology of DEEs and the prospects for applying novel antiepileptic drugs in DEEs. It aims to optimize treatment plans, emphasize individualized and precise diagnosis and treatment, and provide theoretical support for improving understanding and management of this rare epilepsy disease.

Authors

Publication Details

Journal
Advances in Clinical Medicine
Published
2025-01-01
DOI
https://doi.org/10.12677/acm.2025.151002
Primary Topic
Epilepsy research and treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Research Progress on Precise Diagnosis and Treatment of Developmental and Epileptic Encephalopathies

涵 杨
Advances in Clinical Medicine
Epilepsy research and treatment
article

Research Progress on Precise Diagnosis and Treatment of Developmental and Epileptic Encephalopathies

涵 杨
article en

Abstract

发育性癫痫性脑病(developmental and epilepsy encephalopathies, DEEs)是指起病于发育期,以精神运动发育迟缓或倒退为特征的一组癫痫性脑病综合征。DEEs病因及致病机制复杂,遗传因素占据主导地位。当前,病因驱动治疗已成为制定DEEs管理方案的核心,个别综合征亦有特定的药物适应症。本文综述了目前DEEs的遗传学病因及新型抗癫痫药物在DEEs中的应用前景。旨在优化治疗方案,强调个体化精准诊疗,为提高对这一罕见癫痫疾病的理解和管理提供理论支持。Developmental and epileptic encephalopathy (DEEs) refers to a group of epileptic encephalopathy syndromes that begin in the developmental period and are characterized by development delay or regression. The etiology and pathogenesis of DEEs are complex, with genetic factors dominating. Currently, etiology-driven treatment has become the core of DEEs management, and certain syndromes also have specific drug indications. This article reviews the current genetic etiology of DEEs and the prospects for applying novel antiepileptic drugs in DEEs. It aims to optimize treatment plans, emphasize individualized and precise diagnosis and treatment, and provide theoretical support for improving understanding and management of this rare epilepsy disease.

Advances in Clinical MedicineVol. 15(01)
Openalex Percentile: Top 99%
Epilepsy research and treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Research Progress on Precise Diagnosis and Treatment of Developmental and Epileptic Encephalopathies — 涵 杨 · Advances in Clinical Medicine (2025) | TGRS Research Map | TGRS