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Updated: Aug 11, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Rasmussen encephalitis with active inflammation and delayed seizures onset
I Korn-Lubetzki1, C G Bien, J Bauer
1Neurological Service, Department of Pediatrics, Bikur Cholim Hospital, Jerusalem, Israel. ikl@md.huji.ac.il
Abstract:
Severe focal epilepsy is regarded as a clinical hallmark of Rasmussen encephalitis (RE). The authors report two children with progressive hemiparesis, contralateral hemispheric atrophy, and pathologic features characteristic for RE. At histologic diagnosis and over several months, neither patient experienced seizures. The report enlarges the clinical spectrum of RE and suggests that seizures are not an obligatory presenting symptom of the disorder.
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