Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

Leu C., de Kovel C. G. F., Zara F., Striano P., Pezzella M., Robbiano A., ...Daha Fazla

EPILEPSIA, cilt.53, sa.2, ss.308-318, 2012 (SCI-Expanded) identifier identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 53 Sayı: 2
  • Basım Tarihi: 2012
  • Doi Numarası: 10.1111/j.1528-1167.2011.03379.x
  • Dergi Adı: EPILEPSIA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.308-318
  • Anahtar Kelimeler: Genetic generalized epilepsy, Complex inheritance, Absence seizure, Myoclonic seizure, Linkage analysis, JUVENILE MYOCLONIC EPILEPSY, CHILDHOOD ABSENCE EPILEPSY, COMPLEX TRAITS, I ERROR, SEIZURES, HETEROGENEITY, ASSOCIATION, FAMILIES, CHROMOSOME-6, ARCHITECTURE
  • Acıbadem Mehmet Ali Aydınlar Üniversitesi Adresli: Hayır

Özet

Purpose: Genetic generalized epilepsies (GGEs) have a lifetime prevalence of 0.3% with heritability estimates of 80%. A considerable proportion of families with siblings affected by GGEs presumably display an oligogenic inheritance. The present genome-wide linkage meta-analysis aimed to map: (1) susceptibility loci shared by a broad spectrum of GGEs, and (2) seizure typerelated genetic factors preferentially predisposing to either typical absence or myoclonic seizures, respectively.