Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation

Kesim Y. F., Uzun G. A., Yucesan E., Tuncer F. N., Ozdemir O., Bebek N., ...More

EPILEPSY RESEARCH, vol.120, pp.73-78, 2016 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 120
  • Publication Date: 2016
  • Doi Number: 10.1016/j.eplepsyres.2015.12.006
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.73-78
  • Keywords: Lateral temporal lobe epilepsy (LTLE), Autosomal Dominant Lateral Temporal, Epilepsy (ADLTE), Idiopathic Partial Epilepsy with Auditory, Features (IPEAF), LGI1, De novo Mutation, Auditory aura, DOMINANT PARTIAL EPILEPSY, IDIOPATHIC PARTIAL EPILEPSY, FEATURES, FAMILIES, GENE, SEIZURES, REPEAT, ADPEAF, ADLTE, RAT
  • Istanbul University Affiliated: Yes


Autosomal dominant lateral temporal lobe epilepsy (ADLTE) is an autosomal dominant epileptic syndrome characterized by focal seizures with auditory or aphasic symptoms. The same phenotype is also observed in a sporadic form of lateral temporal lobe epilepsy (LTLE), namely idiopathic partial epilepsy with auditory features (IPEAF). Heterozygous mutations in LGI1 account for up to 50% of ADLTE families and only rarely observed in IPEAF cases. In this study, we analysed a cohort of 26 individuals with LTLE diagnosed according to the following criteria: focal epilepsy with auditory aura and absence of cerebral lesions on brain MRI. All patients underwent clinical, neuroradiological and electroencephalography examinations and afterwards they were screened for mutations in LGI1 gene. The single LGI1 mutation identified in this study is a novel missense variant (NM_005097.2: c.1013T>C; p.Phe338Ser) observed de novo in a sporadic patient. This is the first study involving clinical analysis of a LTLE cohort from Turkey and genetic contribution of LGI1 to ADLTE phenotype. Identification of rare LGI1 gene mutations in sporadic cases supports diagnosis as ADTLE and draws attention to potential familial clustering of ADTLE in suggestive generations, which is especially important for genetic counselling. (C) 2015 Elsevier B.V. All rights reserved.