SINDROMI OCULOCEREBRALI ED EPILESSIA

Translated title of the contribution: Oculocerebral syndromes and epilepsy

G. Capocchi, A. Rossi, R. Guerrini

Research output: Contribution to journalArticlepeer-review

Abstract

The clinical, EEG and tomographic characteristics of 14 subjects affected by congenital ocular malformation were studied. In all cases mental retardation was present with associated alteration of language and motor impairment. The EEG in all cases showed an absence of alpha rhythms in the posterior areas and in 10 cases interictal paroxysmal abnormalities. Such anomalies whether unilateral or bilateral prefer the occipital areas. The constant presence of mental retardation, the elevated number of subjects with focal EEG finding (10 cases), and with evidence of various malformations with CT in 5 cases, were not accompanied by a significant association with epilepsy. Effectively only 3 patients present epileptic seizures and only one of them has CT lesions.

Translated title of the contributionOculocerebral syndromes and epilepsy
Original languageItalian
Pages (from-to)147-150
Number of pages4
JournalBollettino - Lega Italiana contro l'Epilessia
VolumeNO. 45-46
Publication statusPublished - 1984

ASJC Scopus subject areas

  • Clinical Neurology

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