258 top medical experts on Rolandic Epilepsy across 42 countries and 18 U.S. states, including 102 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Rolandic Epilepsy: 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)
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Epileptic Syndromes (1,333), Partial Epilepsies (2,698).
  4. Clinical Trials ClinicalTrials.gov : at least 17 including 7 Completed, 3 Recruiting
  5. Synonyms: Benign Childhood Epilepsy With Centro-Temporal Spikes,  Benign Epilepsy With Centrotemporal Spikes,  Benign Rolandic Epilepsy of Childhood,  Centrotemporal Epilepsy,  Rolands Epilepsy,  Sylvian Epilepsy


  

        

                    


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