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Importance of Genetic Testing in Children With Generalized Epilepsy.
Heebner, Madison; Mainali, Gayatra; Wei, Sharon; Kumar, Ashutosh; Naik, Sunil; Pradhan, Sandeep; Kandel, Prakash; Tencer, Jaclyn; Carney, Paul; Paudel, Sita.
Afiliação
  • Heebner M; Neurology, Penn State College of Medicine, Hershey, USA.
  • Mainali G; Pediatric Neurology, Penn State Health Milton S. Hershey Medical Center, Hershey, USA.
  • Wei S; Neurology, Penn State University, Hershey, USA.
  • Kumar A; Pediatric Neurology, Penn State Health Milton S. Hershey Medical Center, Hershey, USA.
  • Naik S; Pediatric Neurology, Penn State Health Milton S. Hershey Medical Center, Hershey, USA.
  • Pradhan S; Biostatistics, Penn State College of Medicine, Hershey, USA.
  • Kandel P; Biostatistics, Penn State College of Medicine, Hershey, USA.
  • Tencer J; Pediatric Neurology, Penn State Health Milton S. Hershey Medical Center, Hershey, USA.
  • Carney P; Pediatrics and Neurology, University of Missouri, Columbia, USA.
  • Paudel S; Pediatric Neurology, Penn State Health Milton S. Hershey Medical Center, Hershey, USA.
Cureus ; 16(5): e59991, 2024 May.
Article em En | MEDLINE | ID: mdl-38854234
ABSTRACT

INTRODUCTION:

Epilepsy is a neurological disorder characterized by the predisposition for recurrent unprovoked seizures. It can broadly be classified as focal, generalized, unclassified, and unknown in its onset. Focal epilepsy originates in and involves networks localized to one region of the brain. Generalized epilepsy engages broader, more diffuse networks. The etiology of epilepsy can be structural, genetic, infectious, metabolic, immune, or unknown. Many generalized epilepsies have presumed genetic etiologies. The aim of this study is to compare the role of genetic testing to brain MRI as diagnostic tools for identifying the underlying causes of idiopathic (genetic) generalized epilepsy (IGE).

METHODS:

 We evaluated the diagnostic yield of these two categories in children diagnosed with IGE. Data collection was completed using ICD10 codes filtered by TriNetX to select 982 individual electronic medical records (EMRs) of children in the Penn State Children's Hospital who received a diagnosis of IGE. The diagnosis was confirmed after reviewing the clinical history and electroencephalogram (EEG) data for each patient.

RESULTS:

From this dataset, neuroimaging and genetic testing results were gathered. A retrospective chart review was done on 982 children with epilepsy, of which 143 (14.5%) met the criteria for IGE. Only 18 patients underwent genetic testing. Abnormalities that could be a potential cause for epilepsy were seen in 72.2% (13/18) of patients with IGE and abnormal genetic testing, compared to 30% (37/123) for patients who had a brain MRI with genetic testing.

CONCLUSION:

This study suggests that genetic testing may be more useful than neuroimaging for identifying an etiological diagnosis of pediatric patients with IGE.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos