Neonatal Epileptic Encephalopathies

被引:3
|
作者
Ahmad, Samiya Fatima [1 ,2 ]
Ahmed, Kaashif Aqeeb [1 ,2 ,3 ]
Ng, Yu-Tze [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Pediat, 315 N San Saba St,Suite 1135, San Antonio, TX 78207 USA
[2] Childrens Hosp San Antonio, San Antonio, TX USA
[3] Pediatrix Med Grp San Antonio, San Antonio, TX USA
关键词
MIGRATING PARTIAL SEIZURES; 5TH DAY FITS; EARLY MYOCLONIC ENCEPHALOPATHY; KCNQ2; ENCEPHALOPATHY; ANTIEPILEPTIC DRUGS; MUTATIONS; INFANCY; EPIDEMIOLOGY; PHENOTYPE; EXPANSION;
D O I
10.1016/j.spen.2021.100880
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The majority of neonatal seizures are related to common diagnoses, including hypoxic-ischemic encephalopathy and intraventricular hemorrhage. While relatively uncommon, neonatal epileptic encephalopathies represent an important group of neonatal seizure disorders that require immediate diagnosis and intervention. In this review, we provide a summary of the benign and severe neonatal epilepsy syndromes. While benign epilepsy syndromes have favorable prognoses, rapid and accurate diagnosis may prevent an unnecessarily long course of antiseizure medications. The severe epilepsy syndromes may be related to a number of underlying genetic disorders and often carry a poor prognosis. Herein we review diagnostic and therapeutic strategies, and provide a set or algorithms for said purposes. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页数:9
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