Abstract

Introduction: Childhood epilepsy is one of the most common neurological problems. The transferrin isoelectric focusing (TIEF) test is a screening test for congenital disorders of glycosylation (CDG). We identified abnormal TIEF test in children with epilepsy in our epilepsy genetics clinic. To determine if an abnormal TIEF test is associated with anti-epileptic medications or abnormal liver functions, we performed a retrospective cohort study. Methods: This study was performed between January 2012 and March 2020. Electronic patient charts were reviewed. Standard non-parametric statistical tests were applied using R statistical software. Fischer’s exact test was used for comparisons. Results: There were 206 patients. The TIEF test was abnormal in 11% (23 out of 206) of the patients. Nine patients were diagnosed with CDG: PMM2-CDG (n = 5), ALG3-CDG (n = 1), ALG11-CDG (n = 2), SLC35A2-CDG (n = 1). We report 51 different genetic diseases in 84 patients. Two groups, (1) abnormal TIEF test; (2) normal TIEF test, showed statistically significant differences for abnormal liver functions and for valproic acid treatment. Conclusion: The TIEF test guided CDG diagnosis in 2.9% of the patients. Due to the high prevalence of CDG (4.4%) in childhood epilepsy, the TIEF test might be included into the diagnostic investigations to allow earlier and cost-effective diagnosis.

Highlights

  • Childhood epilepsy is one of the most common neurological problems

  • We identified an abnormal transferrin isoelectric focusing (TIEF) test in children with epilepsy in our epilepsy genetics clinic who were seen for diagnostic investigations

  • All patients with abnormal TIEF tests are summarized for their clinical features, seizure history, anti-epileptic medications, liver function tests, and TIEF tests in

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Summary

Introduction

Childhood epilepsy is one of the most common neurological problems. The origin of epilepsy is known in about one-third of the children. There are numerous diagnostic investigations for childhood epilepsy. Some of these investigations are performed in pediatric, genetic, and neurology clinics to investigate the underlying etiologies for appropriate management. Metabolic investigations include plasma amino acids, acylcarnitine profile, total and free carnitines, homocysteine, transferrin isoelectric focusing (TIEF) tests, urine organic acids, and urine creatine and guanidinoacetate that may identify some of the treatable inherited metabolic disorders. A targeted generation sequencing panel (TNGSP) for epilepsy, and exome sequencing (ES)

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