Pediatric Neurology
Volume 26, Issue 1 , Pages 26-29, January 2002

Typical and atypical rolandic epilepsy in childhood: a follow-up study

  • Alberto Verrotti, MD, PhD

      Affiliations

    • Corresponding Author InformationCommunications should be addressed to: Dr. Verrotti; Department of Pediatrics-Policlinico Colle Dell’Ara; University G. D’Annunzio; Via dei Vestini, 5; I-66013 Chieti, Italy
    • Department of Pediatrics; University of Chieti; Chieti, Italy
  • ,
  • Giuseppe Latini, MD

      Affiliations

    • Department of Pediatrics; “Di Summa” Hospital; Brindisi, Italy
  • ,
  • Daniela Trotta, MD

      Affiliations

    • Department of Pediatrics; University of Chieti; Chieti, Italy
  • ,
  • Raffaella Giannuzzi, MD

      Affiliations

    • Department of Pediatrics; “Di Summa” Hospital; Brindisi, Italy
  • ,
  • Rocco Cutarella, MD

      Affiliations

    • Department of Neurology; San Valentino Hospital, San Valentino, Italy
  • ,
  • Guido Morgese, MD

      Affiliations

    • Department of Pediatrics; University of Sienna; Sienna, Italy
  • ,
  • Francesco Chiarelli, MD

      Affiliations

    • Department of Pediatrics; University of Chieti; Chieti, Italy

Received 16 May 2001; accepted 30 July 2001.

Abstract 

Atypical features of rolandic epilepsy are not uncommon, although the long-term prognosis of this condition is not known. Eighty-five children (50 male and 35 female) attending the Department of Pediatrics of the University of Chieti, the Department of Pediatrics of Brindisi Hospital, and the Department of Neurology of San Valentino Hospital were selected for the study; these patients were subdivided into two groups according to their clinical presentation. Group A consisted of children who suffered from typical rolandic epilepsy and Group B consisted of children with atypical features of rolandic epilepsy. All patients of both groups were re-evaluated after at least 8 years from the first evaluation, and the frequency of seizures and the response to treatment were similar in the two groups of children. In spite of this fact, in patients who suffered from atypical rolandic epilepsy, we found a significantly higher percentage of learning and behavioral disabilities than in children affected by the classical form of rolandic epilepsy (45.5% vs 7.8%; P < 0.0001). In conclusion, atypical rolandic epilepsy seems to be associated with a high percentage of learning and behavioral disorders.

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PII: S0887-8994(01)00353-8

Pediatric Neurology
Volume 26, Issue 1 , Pages 26-29, January 2002