Literature DB >> 33279965

Developmental and epileptic encephalopathies: what we do and do not know.

Nicola Specchio1, Paolo Curatolo2.   

Abstract

Developmental encephalopathies, including intellectual disability and autistic spectrum disorder, are frequently associated with infant epilepsy. Epileptic encephalopathy is used to describe an assumed causal relationship between epilepsy and developmental delay. Developmental encephalopathies pathogenesis more independent from epilepsy is supported by the identification of several gene variants associated with both developmental encephalopathies and epilepsy, the possibility for gene-associated developmental encephalopathies without epilepsy, and the continued development of developmental encephalopathies even when seizures are controlled. Hence, 'developmental and epileptic encephalopathy' may be a more appropriate term than epileptic encephalopathy. This update considers the best studied 'developmental and epileptic encephalopathy' gene variants for illustrative support for 'developmental and epileptic encephalopathy' over epileptic encephalopathy. Moreover, the interaction between epilepsy and developmental encephalopathies is considered with respect to influence on treatment decisions. Continued research in genetic testing will increase access to clinical tests, earlier diagnosis, better application of current treatments, and potentially provide new molecular-investigated treatments.
© The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  developmental and epileptic encephalopathy; encephalopathy; epileptic seizures; infant; neurodevelopment disorders

Mesh:

Year:  2021        PMID: 33279965     DOI: 10.1093/brain/awaa371

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  12 in total

1.  Novel Variant Expands the Clinical Spectrum of CUX2-Associated Developmental and Epileptic Encephalopathies.

Authors:  Feng Zhang; Fuwei Li; Fujian Chen; Jinrong Huang; Qiong Luo; Xilong Du; Jiapeng Zhou; Weiyue Gu; Kaishou Xu
Journal:  Front Genet       Date:  2022-07-01       Impact factor: 4.772

2.  Epilepsy surgery in PCDH 19 related developmental and epileptic encephalopathy: A case report.

Authors:  Lakshmi Nagarajan; Soumya Ghosh; Jason Dyke; Sharon Lee; Jonathan Silberstein; Dimitar Azmanov; Warne Richard
Journal:  Epilepsy Behav Rep       Date:  2022-07-06

Review 3.  Genetic analysis of developmental and epileptic encephalopathy caused by novel biallelic SZT2 gene mutations in three Chinese Han infants: a case series and literature review.

Authors:  Sai Yang; Li-Ming Yang; Hong-Mei Liao; Hong-Jun Fang; Ze-Shu Ning; Cai-Shi Liao; Li-Wen Wu
Journal:  Neurol Sci       Date:  2022-03-29       Impact factor: 3.830

4.  SCN8A Encephalopathy: Case Report and Literature Review.

Authors:  Hueng-Chuen Fan; Hsiu-Fen Lee; Ching-Shiang Chi
Journal:  Neurol Int       Date:  2021-04-01

5.  De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures.

Authors:  Beryl Royer-Bertrand; Marine Jequier Gygax; Katarina Cisarova; Jill A Rosenfeld; Jennifer A Bassetti; Oana Moldovan; Emily O'Heir; Lindsay C Burrage; Jake Allen; Lisa T Emrick; Emma Eastman; Camille Kumps; Safdar Abbas; Geraldine Van Winckel; Nadia Chabane; Elaine H Zackai; Sebastien Lebon; Beth Keena; Elizabeth J Bhoj; Muhammad Umair; Dong Li; Kirsten A Donald; Andrea Superti-Furga
Journal:  Mol Autism       Date:  2021-10-26       Impact factor: 7.509

6.  Keeping up with KCNQ2: A New Model of Epileptic Encephalopathy.

Authors:  Samantha Bottom-Tanzer; Chris Dulla
Journal:  Epilepsy Curr       Date:  2022-03-11       Impact factor: 7.500

7.  Tubulinopathy Presenting as Developmental and Epileptic Encephalopathy.

Authors:  Kun-Long Hung; Jyh-Feng Lu; Da-Jyun Su; Su-Jin Hsu; Lee-Chin Wang
Journal:  Children (Basel)       Date:  2022-07-23

Review 8.  CDKL5 deficiency disorder: molecular insights and mechanisms of pathogenicity to fast-track therapeutic development.

Authors:  Nicole J Van Bergen; Sean Massey; Anita Quigley; Ben Rollo; Alexander R Harris; Robert M I Kapsa; John Christodoulou
Journal:  Biochem Soc Trans       Date:  2022-08-31       Impact factor: 4.919

9.  Diagnostic Yield and Cost-Effectiveness of "Dynamic" Exome Analysis in Epilepsy with Neurodevelopmental Disorders: A Tertiary-Center Experience in Northern Italy.

Authors:  Costanza Varesio; Simone Gana; Alessia Asaro; Elena Ballante; Raffaella Fiamma Cabini; Elena Tartara; Michela Bagnaschi; Ludovica Pasca; Marialuisa Valente; Simona Orcesi; Cristina Cereda; Pierangelo Veggiotti; Renato Borgatti; Enza Maria Valente; Valentina De Giorgis
Journal:  Diagnostics (Basel)       Date:  2021-05-25

10.  Application of High-Frequency Oscillations on Scalp EEG in Infant Spasm: A Prospective Controlled Study.

Authors:  Lisi Yan; Lin Li; Jin Chen; Li Wang; Li Jiang; Yue Hu
Journal:  Front Hum Neurosci       Date:  2021-06-10       Impact factor: 3.169

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