Rasmussen’s encephalitis with adult onset

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Abstract

Rasmussen’s encephalitis (RE) is a rare inflammatory brain disease characterized by severe intractable epilepsy and unilateral progressive motor defect associated with contralateral hemispheric atrophy. The authors present clinical features, EEG and MRI data and results of effective treatment of patient with adult onset RE. Despite the predominance of RE in children, stressed is the necessity of taking into consideration this condition in adults as well in differential diagnostics of intractable epilepsies.

 
 

About the authors

Aleksey S. Kotov

M.F. Vladimirsky Moscow Regional Research and Clinical Institute

Email: kotovsv@yandex.ru
ORCID iD: 0000-0003-2988-5706

D. Sci. (Med.), Head, Neurological department in the Science section, Professor, Department of neurology

Россия, 129110, Russia, Moscow, Shchepkina str., 61/2

I. G. Rudakova

Moscow Regional Research Clinical Institute

Email: kotovsv@yandex.ru
Россия, Moscow

Sergey V. Kotov

M.F. Vladimirsky Moscow Regional Research and Clinical Institute

Email: kotovsv@yandex.ru
Россия, Moscow

Yu. A. Belova

Moscow Regional Research Clinical Institute

Author for correspondence.
Email: kotovsv@yandex.ru
Россия, Moscow

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Copyright (c) 2008 Kotov A.S., Rudakova I.G., Kotov S.V., Belova Y.A.

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