U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from MedGen

Epilepsy, Rolandic

An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and DYSARTHRIA. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41)

Year introduced: 1997

PubMed search builder options

Subheadings:

Tree Number(s): C10.228.140.490.360.280, C10.228.140.490.493.250

MeSH Unique ID: D019305

Entry Terms:

  • Epilepsies, Rolandic
  • Rolandic Epilepsies
  • Rolandic Epilepsy
  • Sylvian Epilepsy
  • Epilepsy, Sylvian
  • Rolands Epilepsy
  • Epilepsy, Rolands
  • Benign Rolandic Epilepsy
  • Epilepsy, Benign Rolandic
  • Rolandic Epilepsy, Benign
  • Benign Rolandic Epilepsy of Childhood
  • Epilepsy, Centrotemporal
  • Centrotemporal Epilepsies
  • Epilepsies, Centrotemporal
  • Centralopathic Epilepsy
  • Centralopathic Epilepsies
  • Epilepsies, Centralopathic
  • Epilepsy, Centralopathic
  • Centrotemporal Epilepsy
  • BECTS
  • Benign Epilepsy With Centrotemporal Spikes
  • Benign Epilepsy Of Childhood With Centrotemporal Spikes
  • Temporal-Central Focal Epilepsy
  • Epilepsies, Temporal-Central Focal
  • Epilepsy, Temporal-Central Focal
  • Focal Epilepsies, Temporal-Central
  • Focal Epilepsy, Temporal-Central
  • Temporal Central Focal Epilepsy
  • Temporal-Central Focal Epilepsies
  • Benign Childhood Epilepsy With Centro-Temporal Spikes
  • Benign Childhood Epilepsy With Centro Temporal Spikes
  • BCECTS

Previous Indexing:

Supplemental Content

Loading ...