A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy

Hiltrud Muhle, Ines Steinich, Sarah Von Spiczak, Andre Franke, Yvonne Weber, Holger Lerche, Michael Wittig, Simone Heidemann, Arvid Suls, Peter De Jonghe, Carla Marini, Renzo Guerrini, Ingrid E. Scheffer, Samuel F. Berkovic, Ulrich Stephani, Reiner Siebert, Thomas Sander, Ingo Helbig, Holger Tönnies

Research output: Contribution to journalArticlepeer-review


Early onset absence epilepsy (EOAE) starting before the age of 4 years constitutes a rare subgroup of the idiopathic generalized epilepsies (IGEs). A strong genetic component in IGE has been suggested by twin and family studies. We describe a boy with absence seizures starting at the age of 9 months whose parents both had childhood absence epilepsy. A 192-kb duplication in 1q21.3 was identified in the proband and his father, encompassing the gene CHRNB2 coding for the β-2 subunit of the nicotinic acetylcholine receptor and the gene ADAR coding for adenosine deaminase, an enzyme responsible for RNA editing. Both are candidate genes for seizure disorders. The duplication was not identified in 191 independent IGE patients (93 EOAE; 98 classical IGE) or in 1,157 population controls.

Original languageEnglish
Pages (from-to)2453-2456
Number of pages4
Issue number12
Publication statusPublished - Dec 2010


  • 1q21.3 duplication
  • Absence epilepsy
  • ADAR
  • CHRNB2
  • Early onset absence seizures
  • Epilepsy genetics

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology


Dive into the research topics of 'A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy'. Together they form a unique fingerprint.

Cite this