Epilepsy 2022
DOI: 10.36255/exon-publications-epilepsy-neurodevelopmental-disorders
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Overlap Between Epilepsy and Neurodevelopmental Disorders: Insights from Clinical and Genetic Studies

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Cited by 15 publications
(21 citation statements)
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“…For instance, some chromosomal abnormalities, such as 5q14.3 and 7p22.3, were found in both ADHD and epilepsy [ 108 , 109 ]. Likewise, several single nucleotide polymorphisms (SNPs), including myocyte enhancer factor 2 (MEF2C)-related disorders and methyl-CpG binding protein 2 (MECP2), were also found to have a high rate in children with ADHD and CWE [ 110 ]. A growing body of genetic studies suggested a significant familial liability for epilepsy and comorbid ADHD in children with a history of maternal ADHD [ 99 ] and epilepsy [ 111 ], suggesting familial clusters of that ADHD and epilepsy.…”
Section: Adhd and Epilepsy: Mechanisms Of Associationmentioning
confidence: 99%
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“…For instance, some chromosomal abnormalities, such as 5q14.3 and 7p22.3, were found in both ADHD and epilepsy [ 108 , 109 ]. Likewise, several single nucleotide polymorphisms (SNPs), including myocyte enhancer factor 2 (MEF2C)-related disorders and methyl-CpG binding protein 2 (MECP2), were also found to have a high rate in children with ADHD and CWE [ 110 ]. A growing body of genetic studies suggested a significant familial liability for epilepsy and comorbid ADHD in children with a history of maternal ADHD [ 99 ] and epilepsy [ 111 ], suggesting familial clusters of that ADHD and epilepsy.…”
Section: Adhd and Epilepsy: Mechanisms Of Associationmentioning
confidence: 99%
“…ADHD is a neurobiological disorder that encompasses several biological dimensions with multifactorial interactions. Thus, ADHD and epilepsy may share certain aspects of biological dimensions, despite the distinct clinical phenotypes [ 110 ]. Therefore, comprehensive omics data analysis is needed to investigate the biological overlap between ADHD and epilepsy.…”
Section: Adhd and Epilepsy: Mechanisms Of Associationmentioning
confidence: 99%
“…In a systematic review and meta-analyses from 2015, estimates of ASD range from 11% for 22q11.2 deletion syndrome to 61% in females with RTT [34] . For all syndromes, odds ratios showed that people with ASD have a higher risk of genetic abnormalities than the general population.…”
Section: The Chronic Dynamic Systemic Encephalopathy Frameworkmentioning
confidence: 99%
“…It is also suggested that in children with ADHD, epilepsy is three times more often than in the general population; thus it is assumed that ADHD and epilepsy are co-occurring conditions (e.g., Socanski et al, 2013). However, Shimizu et al (2022) believed that the background of epilepsy and neurodevelopmental conditions are biological and shared, which brings the question of the risk factors for epilepsy, such as seizures, epileptic status, and antiseizure therapy, have any imprint in ADHD emergence and if the development of the disorder in children with epilepsy can be prevented with satisfactory seizure control (Chidi et al, 2014; Drechsler et al, 2020; Shimizu et al, 2022). There is also a fact that children with recently diagnosed epilepsy at the early stages of the disease are 2.5 times more likely to develop ADHD symptoms than healthy controls (Besag et al, 2016).…”
Section: Introductionmentioning
confidence: 99%
“…The International Classification of Diseases 11th Revision (ICD-11; World Health Organization [WHO], 2019) defines ADHD as a disorder with onset during the developmental period, typically early to mild childhood, with the same patterns of inattention and symptoms of hyperactivity/impulsivity. In addition, the ICD-11 clearly distinguishes between ADHD disorder and symptoms of inattention, hyperactivity, and impulsivity, which may be caused by the effects of drugs, including antiseizure medications (ASMs; Shimizu et al, 2022). In this regard, ASMs may lead to additional behavioral and attention problems (e.g., Davis et al, 2010).…”
Section: Introductionmentioning
confidence: 99%