Journal of Child Neurology

 

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Journal of Child Neurology, Vol. 17, No. 2 suppl, 2S9-2S22 (2002)
DOI: 10.1177/08830738020170021201

Infantile Spasms and Lennox-Gastaut Syndrome

Edwin Trevathan, MD, MPH

Pediatric Epilepsy Center, Suite 12E47, St. Louis Children's Hospital, St. Louis, MO 63110-1093, trevathan_e{at}kids.wustl.edu

Infantile spasms and Lennox-Gastaut syndrome are rare but are important to child neurologists because of the intractable nature of the seizures and the serious neurologic comorbidities. New antiepileptic drugs offer more alternatives for treating both infantile spasms and Lennox-Gastaut syndrome. Selected children with infantile spasms are candidates for epilepsy surgery. Vagus nerve stimulation, corpus callosotomy, and the ketogenic diet are all options for selected children with Lennox-Gastaut syndrome. The epidemiology, clinical manifestations of the seizures, electroencephalographic characteristics, prognosis, and treatment options are reviewed for infantile spasms and Lennox-Gastaut syndrome. Additional therapies are needed for both infantile spasms and Lennox-Gastaut syndrome as many children fail to achieve adequate seizure control in spite of newer treatments. (J Child Neurol 2002;17:2S9—2S22).


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