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
  • [41] Solving the Molecular Basis of the Developmental and Epileptic Encephalopathies: Are We there Yet?
    Scheffer, Ingrid E.
    EPILEPSY CURRENTS, 2021, 21 (06) : 430 - 432
  • [42] Early-Onset Epileptic Encephalopathies: Ohtahara Syndrome and Early Myoclonic Encephalopathy
    Beal, Jules C.
    Cherian, Koshi
    Moshe, Solomon L.
    PEDIATRIC NEUROLOGY, 2012, 47 (05) : 317 - 323
  • [43] Early infantile epileptic encephalopathy and glycine encephalopathy
    de Dios, JG
    Moya, M
    Pastore, C
    Izura, V
    Carratala, F
    REVISTA DE NEUROLOGIA, 1997, 25 (148) : 1916 - 1918
  • [44] Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice
    Scheffer, Ingrid E.
    Bennett, Caitlin A.
    Gill, Deepak
    de Silva, Michelle G.
    Boggs, Kirsten
    Marum, Justine
    Baker, Naomi
    Palmer, Elizabeth E.
    Howell, Katherine B.
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2023, 65 (01): : 50 - 57
  • [45] STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern
    Saitsu, Hirotomo
    Kato, Mitsuhiro
    Okada, Ippei
    Orii, Kenji E.
    Higuchi, Tsukasa
    Hoshino, Hideki
    Kubota, Masaya
    Arai, Hiroshi
    Tagawa, Tetsuzo
    Kimura, Shigeru
    Sudo, Akira
    Miyama, Sahoko
    Takami, Yuichi
    Watanabe, Toshihide
    Nishimura, Akira
    Nishiyama, Kiyomi
    Miyake, Noriko
    Wada, Takahito
    Osaka, Hitoshi
    Kondo, Naomi
    Hayasaka, Kiyoshi
    Matsumoto, Naomichi
    EPILEPSIA, 2010, 51 (12) : 2397 - 2405
  • [46] Is Precision Therapy in Infantile-Onset Epileptic Encephalopathies Still Too Far to Call Upon?
    Falsaperla, Raffaele
    Sortino, Vincenzo
    Pavone, Piero
    APPLIED SCIENCES-BASEL, 2025, 15 (05):
  • [47] KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum
    Bonardi, Claudia M.
    Heyne, Henrike O.
    Fiannacca, Martina
    Fitzgerald, Mark P.
    Gardella, Elena
    Gunning, Boudewijn
    Olofsson, Kern
    Lesca, Gaetan
    Verbeek, Nienke
    Stamberger, Hannah
    Striano, Pasquale
    Zara, Federico
    Mancardi, Maria M.
    Nava, Caroline
    Syrbe, Steffen
    Buono, Salvatore
    Baulac, Stephanie
    Coppola, Antonietta
    Weckhuysen, Sarah
    Schoonjans, An-Sofie
    Ceulemans, Berten
    Sarret, Catherine
    Baumgartner, Tobias
    Muhle, Hiltrud
    des Portes, Vincent
    Toulouse, Joseph
    Nougues, Marie-Christine
    Rossi, Massimiliano
    Demarquay, Genevieve
    Ville, Dorothee
    Hirsch, Edouard
    Maurey, Helene
    Willems, Marjolaine
    de Bellescize, Julitta
    Altuzarra, Cecilia Desmettre
    Villeneuve, Nathalie
    Bartolomei, Fabrice
    Picard, Fabienne
    Hornemann, Frauke
    Koolen, David A.
    Kroes, Hester Y.
    Reale, Chiara
    Fenger, Christina D.
    Tan, Wen-Hann
    Dibbens, Leanne
    Bearden, David R.
    Moller, Rikke S.
    Rubboli, Guido
    BRAIN, 2021, 144 : 3635 - 3650
  • [48] Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study
    Cavirani, Benedetta
    Spagnoli, Carlotta
    Caraffi, Stefano Giuseppe
    Cavalli, Anna
    Cesaroni, Carlo Alberto
    Cutillo, Gianni
    De Giorgis, Valentina
    Frattini, Daniele
    Marchetti, Giulia Bruna
    Masnada, Silvia
    Peron, Angela
    Rizzi, Susanna
    Varesio, Costanza
    Spaccini, Luigina
    Vignoli, Aglaia
    Canevini, Maria Paola
    Veggiotti, Pierangelo
    Garavelli, Livia
    Fusco, Carlo
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (02)
  • [49] The utility of whole exome sequencing for identification of the molecular etiology in autosomal recessive developmental and epileptic encephalopathies
    Isik, Esra
    Yilmaz, Sanem
    Atik, Tahir
    Aktan, Gul
    Onay, Huseyin
    Gokben, Sarenur
    Ozkinay, Ferda
    NEUROLOGICAL SCIENCES, 2020, 41 (12) : 3729 - 3739
  • [50] Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy
    Chong, Shuk Ching
    Cao, Ye
    Fung, Eva L. W.
    Kleppe, Soledad
    Gripp, Karen W.
    Hertecant, Jozef
    El-Hattab, Ayman W.
    Suleiman, Jehan
    Clark, Gary
    von Allmen, Gretchen
    Rodziyevska, Olga
    Lewis, Richard A.
    Rosenfeld, Jill A.
    Dong, Jie
    Wang, Xia
    Miller, Marcus J.
    Bi, Weimin
    Liu, Pengfei
    Scaglia, Fernando
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191 (03) : 776 - 785