Molecular bases and clinical spectrum of early infantile epileptic encephalopathies

被引:35
|
作者
Asher, Y. Jane Tavyev [1 ]
Scaglia, Fernando [2 ]
机构
[1] Cedars Sinai Med Ctr, Dept Pediat, Los Angeles, CA 90048 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Clin Care Ctr, Houston, TX 77030 USA
关键词
Epilepsy; Infantile epileptic encephalopathy; Infantile spasms; SYNAPTIC VESICLE FUSION; EARLY MYOCLONIC ENCEPHALOPATHY; LINKED MENTAL-RETARDATION; SUPPRESSION-BURST PATTERN; LENNOX-GASTAUT SYNDROME; ALPHA-II-SPECTRIN; DE-NOVO MUTATIONS; STXBP1; MUTATIONS; OHTAHARA-SYNDROME; WEST-SYNDROME;
D O I
10.1016/j.ejmg.2012.04.002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Epilepsy can be a challenging diagnosis to make in the neonatal and infantile periods. Seizures in this age group may be due to a serious underlying cause that results in an epileptic encephalopathy. Early infantile epileptic encephalopathy (EIEE) is a progressive neurologic condition that exhibits concomitant cognitive and motor impairment, and is often associated with severe intellectual disability. This condition belongs to the group of age-dependent epileptic encephalopathies, and thus the clinical and electro-encephalographic features change with age as the central nervous system evolves. The molecular bases and the clinical spectrum associated with the early infantile epileptic encephalopathies continue to expand as new genetic discoveries are made. This review will highlight the molecular etiologies of early infantile epileptic encephalopathy, and the clinical and electro-encephalographic changes that take place in these epileptic phenotypes as the brain develops. (c) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:299 / 306
页数:8
相关论文
共 50 条
  • [21] Chromosomal microarray and exome sequencing in unexplained early infantile epileptic encephalopathies in a highly consanguineous population
    Turkdogan, Dilsad
    Turkyilmaz, Ayberk
    Sager, Gunes
    Ozturk, Gulten
    Unver, Olcay
    Say, Merve
    INTERNATIONAL JOURNAL OF NEUROSCIENCE, 2023, 133 (07) : 683 - 700
  • [22] Epileptic Encephalopathies-Clinical Syndromes and Pathophysiological Concepts
    von Deimling, Markus
    Helbig, Ingo
    Marsh, Eric D.
    CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2017, 17 (02)
  • [23] STXBP1 encephalopathies: Clinical spectrum, disease mechanisms, and therapeutic strategies
    Abramov, Debra
    Guiberson, Noah Guy Lewis
    Burre, Jacqueline
    JOURNAL OF NEUROCHEMISTRY, 2021, 157 (02) : 165 - 178
  • [24] Causes of mortality in early infantile epileptic encephalopathy: A systematic review
    Radaelli, Graciane
    Santos, Francisco de Souza
    Borelli, Wyllians Vendramini
    Pisani, Leonardo
    Nunes, Magda Lahorgue
    Scorza, Fulvio Alexandre
    da Costa, Jaderson Costa
    EPILEPSY & BEHAVIOR, 2018, 85 : 32 - 36
  • [25] Cerebrospinal fluid pterins and neurotransmitters in early severe epileptic encephalopathies
    Duarte, Sofia
    Sanmarti, Francesc
    Gonzalez, Veronica
    Duenas, Belen Perez
    Ormazabal, Aida
    Artuch, Rafael
    Campistol, Jaime
    Garcia-Cazorla, Angels
    BRAIN & DEVELOPMENT, 2008, 30 (02): : 106 - 111
  • [26] Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies
    Heron, Sarah E.
    Ong, Yeh Sze
    Yendle, Simone C.
    McMahon, Jacinta M.
    Berkovic, Samuel F.
    Scheffer, Ingrid E.
    Dibbens, Leanne M.
    EPILEPSIA, 2013, 54 (05) : e86 - e89
  • [27] Genomic Investigation of Infantile and Childhood Epileptic Encephalopathies in Kazakhstan: An Urgent Priority
    Jaxybayeva, Altynshash
    Nauryzbayeva, Alissa
    Khamzina, Assem
    Takhanova, Meruert
    Abilhadirova, Assel
    Rybalko, Anastasia
    Jamanbekova, Kymbat
    FRONTIERS IN NEUROLOGY, 2021, 12
  • [28] Precision Medicine Approaches for Infantile-Onset Developmental and Epileptic Encephalopathies
    Myers, Kenneth A.
    Scheffer, Ingrid E.
    ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2022, 62 : 641 - 662
  • [29] Rett Syndrome Spectrum in Monogenic Developmental-Epileptic Encephalopathies and Epilepsies: A Review
    Spagnoli, Carlotta
    Fusco, Carlo
    Pisani, Francesco
    GENES, 2021, 12 (08)
  • [30] Novel Variant Expands the Clinical Spectrum of CUX2-Associated Developmental and Epileptic Encephalopathies
    Zhang, Feng
    Li, Fuwei
    Chen, Fujian
    Huang, Jinrong
    Luo, Qiong
    Du, Xilong
    Zhou, Jiapeng
    Gu, Weiyue
    Xu, Kaishou
    FRONTIERS IN GENETICS, 2022, 13