Literature DB >> 28548558

The role of genetic testing in epilepsy diagnosis and management.

Yvonne G Weber1, Saskia Biskup2, Katherine L Helbig3, Sarah Von Spiczak4,5, Holger Lerche1.   

Abstract

INTRODUCTION: Epilepsy is a common neurological disorder characterized by recurrent unprovoked seizures. More than 500 epilepsy-associated genes have been described in the literature. Most of these genes play an important role in neuronal excitability, cortical development or synaptic transmission. A growing number of genetic variations have implications on diagnosis and prognostic or therapeutic advice in terms of a personalized medicine. Area covered: The review presents the different forms of genetic epilepsies with respect to their underlying genetic and functional pathophysiology and aims to give advice for recommended genetic testing. Moreover, it discusses ethical and legal guidelines, costs and technical limitations which should be considered. Expert commentary: Genetic testing is an important component in the diagnosis and treatment of many forms of epilepsy.

Entities:  

Keywords:  Genetic counseling; exome; genetic epilepsies; genome; idiopathic; metabolic epilepsies; microarray analysis; next generation sequencing; personalized medicine; precision medicine

Mesh:

Year:  2017        PMID: 28548558     DOI: 10.1080/14737159.2017.1335598

Source DB:  PubMed          Journal:  Expert Rev Mol Diagn        ISSN: 1473-7159            Impact factor:   5.225


  19 in total

1.  Customized multigene panels in epilepsy: the best things come in small packages.

Authors:  Simona Pellacani; Claudia Dosi; Giulia Valvo; Francesca Moro; Serena Mero; Federico Sicca; Filippo Maria Santorelli
Journal:  Neurogenetics       Date:  2019-12-13       Impact factor: 2.660

Review 2.  Individualizing Treatment Approaches for Epileptic Patients with Glucose Transporter Type1 (GLUT-1) Deficiency.

Authors:  Armond Daci; Adnan Bozalija; Fisnik Jashari; Shaip Krasniqi
Journal:  Int J Mol Sci       Date:  2018-01-05       Impact factor: 5.923

3.  Mutation in an alternative transcript of CDKL5 in a boy with early-onset seizures.

Authors:  Dale L Bodian; John M Schreiber; Thierry Vilboux; Alina Khromykh; Natalie S Hauser
Journal:  Cold Spring Harb Mol Case Stud       Date:  2018-06-01

4.  Functional Connectivity and Genetic Profile of a "Double-Cortex"-Like Malformation.

Authors:  Giulia Sprugnoli; Giampaolo Vatti; Simone Rossi; Alfonso Cerase; Alessandra Renieri; Maria A Mencarelli; Federico Zara; Alessandro Rossi; Emiliano Santarnecchi
Journal:  Front Integr Neurosci       Date:  2018-06-12

5.  Agitation and Sugar Craving Related to Epilepsy Seizure.

Authors:  Rania Adel Hameed; Mohammad Reza F Aghdam
Journal:  Case Rep Psychiatry       Date:  2021-05-03

6.  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

7.  Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes.

Authors:  Laura Ortega-Moreno; Beatriz G Giráldez; Victor Soto-Insuga; Rebeca Losada-Del Pozo; María Rodrigo-Moreno; Cristina Alarcón-Morcillo; Gema Sánchez-Martín; Esther Díaz-Gómez; Rosa Guerrero-López; José M Serratosa
Journal:  PLoS One       Date:  2017-11-30       Impact factor: 3.240

8.  Novel and de novo mutations in pediatric refractory epilepsy.

Authors:  Jing Liu; Lili Tong; Shuangshuang Song; Yue Niu; Jun Li; Xiu Wu; Jie Zhang; Clement C Zai; Fang Luo; Jian Wu; Haiyin Li; Albert H C Wong; Ruopeng Sun; Fang Liu; Baomin Li
Journal:  Mol Brain       Date:  2018-09-05       Impact factor: 4.041

9.  Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients.

Authors:  Ana Fernández-Marmiesse; Iria Roca; Felícitas Díaz-Flores; Verónica Cantarín; Mª Socorro Pérez-Poyato; Ana Fontalba; Francisco Laranjeira; Sofia Quintans; Oana Moldovan; Blanca Felgueroso; Montserrat Rodríguez-Pedreira; Rogelio Simón; Ana Camacho; Pilar Quijada; Salvador Ibanez-Mico; Mª Rosario Domingno; Carmen Benito; Rocío Calvo; Antonia Pérez-Cejas; Mª Llanos Carrasco; Feliciano Ramos; Mª Luz Couce; Mª Luz Ruiz-Falcó; Luis Gutierrez-Solana; Margarita Martínez-Atienza
Journal:  Front Neurosci       Date:  2019-11-08       Impact factor: 4.677

10.  The Effect of Protein-Rich Extract from Bombyx Batryticatus against Glutamate-Damaged PC12 Cells Via Regulating γ-Aminobutyric Acid Signaling Pathway.

Authors:  Li-Ying He; Mei-Bian Hu; Ruo-Lan Li; Rong Zhao; Lin-Hong Fan; Li Wang; Wei Peng; Yu-Jie Liu; Chun-Jie Wu
Journal:  Molecules       Date:  2020-01-28       Impact factor: 4.411

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