Literature DB >> 26345167

Obtaining genetic testing in pediatric epilepsy.

Margie A Ream1,2, Anup D Patel1,2.   

Abstract

The steps from patient evaluation to genetic diagnosis remain complicated. We discuss some of the genetic testing methods available along with their general advantages and disadvantages. We briefly review common pediatric epilepsy syndromes with strong genetic association and provide a potentially useful algorithm for genetic testing in drug-resistant epilepsy. We performed an extensive literature review of available information as it pertains to genetic testing and genetics in pediatric epilepsy. If a genetic disorder is suspected as the cause of epilepsy, based on drug resistance, family history, or clinical phenotype, timely diagnosis may reduce overall cost, limit the diagnostic odyssey that can bring much anxiety to families, improve prognostic accuracy, and lead to targeted therapy. Interpretation of complicated results should be performed only in collaboration with geneticists and genetic counselors, unless the ordering neurologist has a strong background in and understanding of genetics. Genetic testing can play an important role in the care provided to patients with epilepsy. Wiley Periodicals, Inc.
© 2015 International League Against Epilepsy.

Entities:  

Keywords:  Diagnosis; Exome sequencing; Next generation sequencing

Mesh:

Substances:

Year:  2015        PMID: 26345167     DOI: 10.1111/epi.13122

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  9 in total

1.  Diagnostic yield of genetic tests in epilepsy: A meta-analysis and cost-effectiveness study.

Authors:  Iván Sánchez Fernández; Tobias Loddenkemper; Marina Gaínza-Lein; Beth Rosen Sheidley; Annapurna Poduri
Journal:  Neurology       Date:  2019-01-04       Impact factor: 9.910

2.  Attitudes Toward Epilepsy Genetics Testing Among Adult and Pediatric Epileptologists-Results of a Q-PULSE Survey.

Authors:  Lindsay Ferraro; John R Pollard; Ingo Helbig
Journal:  Epilepsy Curr       Date:  2016 Jan-Feb       Impact factor: 7.500

3.  Commentary: 2016 Clinical Epilepsia Prize.

Authors:  David T Miller
Journal:  Epilepsia       Date:  2016-08-14       Impact factor: 5.864

4.  Etiologic classification of infantile spasms using positron emission/magnetic resonance imaging and the efficacy of adrenocorticotropic hormone therapy.

Authors:  Haodan Dang; Liping Zou; Jiahe Tian; Jiajin Liu; Xiang Feng; Mu Lin; Baixuan Xu
Journal:  Eur J Nucl Med Mol Imaging       Date:  2020-01-03       Impact factor: 9.236

5.  Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing.

Authors:  Yimin Wang; Xiaonan Du; Rao Bin; Shanshan Yu; Zhezhi Xia; Guo Zheng; Jianmin Zhong; Yunjian Zhang; Yong-Hui Jiang; Yi Wang
Journal:  Sci Rep       Date:  2017-01-11       Impact factor: 4.379

6.  Determining the best candidates for next-generation sequencing-based gene panel for evaluation of early-onset epilepsy.

Authors:  Jiwon Lee; Chung Lee; Chang-Seok Ki; Jeehun Lee
Journal:  Mol Genet Genomic Med       Date:  2020-07-01       Impact factor: 2.183

7.  A Multi-Disciplinary Team Approach to Genomic Testing for Drug-Resistant Epilepsy Patients-The GENIE Study.

Authors:  Lata Vadlamudi; Carmen Maree Bennett; Melanie Tom; Ghusoon Abdulrasool; Kristian Brion; Ben Lundie; Hnin Aung; Chiyan Lau; Jonathan Rodgers; Kate Riney; Louisa Gordon
Journal:  J Clin Med       Date:  2022-07-21       Impact factor: 4.964

8.  Targeted Whole Exome Sequencing in Children With Early-Onset Epilepsy: Parent Experiences.

Authors:  Armaghan Alam; Maksim Parfyonov; Camille Y Huang; Inderpal Gill; Mary B Connolly; Judy Illes
Journal:  J Child Neurol       Date:  2022-08-03       Impact factor: 2.363

9.  Etiology, syndrome diagnosis, and cognition in childhood-onset epilepsy: A population-based study.

Authors:  Arja Sokka; Päivi Olsen; Jarkko Kirjavainen; Maijakaisa Harju; Leea Keski-Nisula; Sari Räisänen; Seppo Heinonen; Reetta Kälviäinen
Journal:  Epilepsia Open       Date:  2017-01-19
  9 in total

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