Abstract
We report a subject in whom Leigh syndrome and partial deficit of cytochrome-c oxidase (COX) were associated with epilepsia partialis continua (EPC). The clinical picture and the frequency of seizures were not modified by several therapeutic attempts with different antiepileptic drugs; however, treatment with ACTH depot induced a long-term reduction in severity of myoclonic jerks.
Translated title of the contribution | Responsiveness of epilepsia partialis continua to ACTH depot treatment in a patient with congenital lactic acidosis |
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Original language | Italian |
Pages (from-to) | 161-162 |
Number of pages | 2 |
Journal | Bollettino - Lega Italiana contro l'Epilessia |
Issue number | 95-96 |
Publication status | Published - 1996 |
ASJC Scopus subject areas
- Clinical Neurology