| Literature DB >> 25051969 |
Alberto Verrotti1, Giulia Loiacono2, Alessandra Rossi2, Armando Tartaro3, Andrea Delli Pizzi3, Giangennaro Coppola4.
Abstract
Schizencephaly is an uncommon malformation of cortical development. Patients with schizencephaly present with a broad range of severe neurologic symptoms including pharmacoresistant epilepsy. Rufinamide is a new antiepileptic drug approved for use as adjunctive therapy of seizures associated with Lennox-Gastaut syndrome and it is also effective for refractory partial seizures. We report 3 cases of pediatric patients aged 7.2, 8.1, and 10.1 years, respectively, with intractable epilepsy associated with bilateral open-lip schizencephaly and septo-optic dysplasia. The follow-up ranged from 3.8 to 4.1 years. In our patients, the introduction of rufinamide as adjunctive drug led to a dramatic decline in the number of seizures and an improvement in EEG epileptic activity without side effects. Rufinamide seems to be efficacious and safe in patients with epileptic encephalopathies associated with pharmacoresistant epilepsy; further and larger clinical reports and controlled studies could confirm the usefulness of this anticonvulsant drug.Entities:
Keywords: antiepileptic drugs; epilepsy; rufinamide; schizencephaly; septo-optic dysplasia
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Year: 2014 PMID: 25051969 DOI: 10.1177/0883073814542951
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987