Risposta al trattamento con ACTH depot in un caso di epilessia parziale continua associata ad acidosi lattica congenita

Translated title of the contribution: Responsiveness of epilepsia partialis continua to ACTH depot treatment in a patient with congenital lactic acidosis

A. Vetro, A. Milici, A. Russello, M. C. Valido, A. Indelicato, M. Elia, G. Amodeo

Research output: Contribution to journalArticlepeer-review

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 contributionResponsiveness of epilepsia partialis continua to ACTH depot treatment in a patient with congenital lactic acidosis
Original languageItalian
Pages (from-to)161-162
Number of pages2
JournalBollettino - Lega Italiana contro l'Epilessia
Issue number95-96
Publication statusPublished - 1996

ASJC Scopus subject areas

  • Clinical Neurology

Fingerprint

Dive into the research topics of 'Responsiveness of epilepsia partialis continua to ACTH depot treatment in a patient with congenital lactic acidosis'. Together they form a unique fingerprint.

Cite this