• Tuğrul Berrin, Yılmaz Hikmet, Vatandaş Gülşen, Bozyiğit Ferda, Balcan Erdal, and Onur Ece.
• Celal Bayar University Faculty of Science and Letter, Molecular Biology.
• Afr Health Sci. 2015 Dec 1; 15 (4): 1204-10.

BackgroundIdiopathic generalized epilepsy (IGE) is an epilepsy form without an underlying brain lesion or neurological indication or symptom. Recent investigations on the genetic origins of IGE and its subtypes report that certain mutations of various ion and non-ion channels genes in the central nervous system may be associated with IGE.PurposeIn this study we evaluated the relation between IGE and S430Y polymorphism in EFHC2 gene in a Turkish population.Material/MethodsThe study enrolled 96 healthy volunteers (47 male, 49 female), served as controls, and 96 IGE patients (41 male, 55 female), IGE diagnosis was confirmed in the neurology department. DNA extractions were performed. The presence of S430Y polymorphism in the exon 9 of EFHC2 gene were analyzed by Real-Time PCR. The findings obtained from the control and patient groups were compared.ResultsIn the patient group there was one heterozygous male with 685 T>C mutation. In the control group, there were two objects with 685 T>C mutation; one heterozygous male, one heterozygous female. 662 G>A mutation was determined in neither controls nor patients.ConclusionIn our series of 96 IGE patients and 96 healthy controls, there was no relation between S430Y polymorphism in EFHC2 gene and IGE presence.

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