Genetic testing for unexplained epilepsy: A review of diagnostic approach, benefits, and referral algorithm

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Abstract

In the last several decades, advances in genetic testing have transformed the diagnostic and therapeutic approach to pediatric epilepsy. However, the interpretation of these genetic tests often requires expert analysis and counseling. For this reason, as our molecular understanding of the linkages between abnormal cerebral physiology and genetics has grown, so too has the field of clinical epilepsy genetics. Here we explore recent advances in genetic testing, describe the benefits of genetic testing in epilepsy, and provide a practice guideline for testing and referrals to specialized epilepsy genetics centers, highlighting the Epilepsy NeuroGenetics Initiative (ENGIN) Clinic and the Center for Epilepsy and Neurodevelopmental Disorders (ENDD) at the Children's Hospital of Philadelphia as an illustration of such a specialized center.

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不明原因癫痫的基因检测:诊断方法、益处和转诊算法综述。
在过去的几十年里,基因检测技术的进步改变了小儿癫痫的诊断和治疗方法。然而,对这些基因检测结果的解释往往需要专家的分析和咨询。因此,随着我们对异常脑生理学和遗传学之间联系的分子认识不断加深,临床癫痫遗传学领域也在不断发展。在此,我们探讨了基因检测的最新进展,描述了癫痫基因检测的益处,并提供了检测和转诊到专业癫痫遗传学中心的实践指南,重点介绍了费城儿童医院的癫痫神经遗传学倡议(ENGIN)诊所和癫痫与神经发育障碍中心(ENDD),以说明此类专业中心的情况。
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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
61
审稿时长
5 days
期刊介绍: Recognized for its probing, comprehensive, and evidence-based reviews, Current Problems in Pediatric and Adolescent Health Care devotes each issue to a timely and practical topic in pediatric medicine, presented by leading authorities in the field. The journal offers readers easily accessible information that enhances professional experience and is pertinent to daily pediatric practice. Each issue''s review article is accompanied by an additional special feature designed to highlight a particular aspect of the topic presented.
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