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
  • [1] Early infantile epileptic encephalopathies
    Fois A.
    Italian Journal of Pediatrics, 40 (Suppl 1) : 1 - 1
  • [2] A genetic diagnostic approach to infantile epileptic encephalopathies
    Kamien, Benjamin A.
    Cardamone, Michael
    Lawson, John A.
    Sachdev, Rani
    JOURNAL OF CLINICAL NEUROSCIENCE, 2012, 19 (07) : 934 - 941
  • [3] The Expanding Clinical Spectrum of Genetic Pediatric Epileptic Encephalopathies
    Shbarou, Rolla
    Mikati, Mohamad A.
    SEMINARS IN PEDIATRIC NEUROLOGY, 2016, 23 (02) : 134 - 142
  • [4] Clinical review of genetic epileptic encephalopathies
    Noh, Grace J.
    Asher, Y. Jane Tavyev
    Graham, John M., Jr.
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2012, 55 (05) : 281 - 298
  • [5] Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation
    Kato, Mitsuhiro
    Yamagata, Takanori
    Kubota, Masaya
    Arai, Hiroshi
    Yamashita, Sumimasa
    Nakagawa, Taku
    Fujii, Takanari
    Sugai, Kenji
    Imai, Kaoru
    Uster, Tami
    Chitayat, David
    Weiss, Shelly
    Kashii, Hirofumi
    Kusano, Ryosuke
    Matsumoto, Ayumi
    Nakamura, Kazuyuki
    Oyazato, Yoshinobu
    Maeno, Mari
    Nishiyama, Kiyomi
    Kodera, Hirofumi
    Nakashima, Mitsuko
    Tsurusaki, Yoshinori
    Miyake, Noriko
    Saito, Kayoko
    Hayasaka, Kiyoshi
    Matsumoto, Naomichi
    Saitsu, Hirotomo
    EPILEPSIA, 2013, 54 (07) : 1282 - 1287
  • [6] Expanding the clinical phenotype and genetic spectrum of GEMIN5 disorders: Early-infantile developmental and epileptic encephalopathies
    Zhang, Jing
    Liu, Xinting
    Zhu, Gang
    Wan, Lin
    Liang, Yan
    Li, Nannan
    Huang, Mingwei
    Yang, Guang
    BRAIN AND BEHAVIOR, 2024, 14 (05):
  • [7] Genes in infantile epileptic encephalopathies
    Depienne, Christel
    Gourfinkel-An, Isabelle
    Baulac, Stephanie
    LeGuern, Eric
    EPILEPSIA, 2010, 51 : 69 - 69
  • [8] Epileptic Encephalopathies in Early Infancy
    Ohtahara S.
    Ohtsuka Y.
    Oka E.
    The Indian Journal of Pediatrics, 1997, 64 (5) : 603 - 612
  • [9] Clinical management of epileptic encephalopathies of childhood and infancy
    Covanis, Athanasios
    EXPERT REVIEW OF NEUROTHERAPEUTICS, 2014, 14 (06) : 687 - 701
  • [10] Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies
    Galanopoulou, Aristea S.
    Moshe, Solomon L.
    NEUROBIOLOGY OF DISEASE, 2015, 79 : 135 - 149