A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2

Epilepsia. 2004 Feb;45(2):190-2. doi: 10.1111/j.0013-9580.2004.39903.x.

Abstract

Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by cortical tremor and generalized seizures, mapped on chromosome 8q24 by Japanese authors. Recently the same phenotype also was reported in European families, with linkage on chromosome 2. We present a new family with suggestion of linkage to chromosome 2p11.1-2q12.2 (lod score value, 1.55). This observation would confirm that BAFME is a worldwide, genetically heterogeneous condition, probably with Japanese families linked to 8q24 and European families to 2p11.1-q12.2.

MeSH terms

  • Adult
  • Aged
  • Chromosomes, Human, Pair 2*
  • Epilepsies, Myoclonic / classification
  • Epilepsies, Myoclonic / genetics*
  • Family Health
  • Female
  • Genetic Linkage*
  • Humans
  • Male
  • Pedigree
  • Phenotype