Intrauterine-Onset Myoclonic Encephalopathy Associated With Cerebral Cortical Dysgenesis

Adre J. du Plessis, Walter E. Kaufmann, William J. Kupsky

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The intrauterine onset of convulsive syndromes has been documented only rarely, and previous reports have lacked detailed neuropathologic description. This report details a case of severe, intractable myoclonic encephalopathy, which, on the basis of severely abnormal paroxysmal fetal movement patterns confirmed by antenatal ultrasound, appears to have been of antenatal onset. The infant suffered an early demise and at autopsy showed features of a severe brain dysgenesis with polymicrogyria and superadded encephaloclastic features. Despite an extensive evaluation, the etiology of this condition remains elusive in our case. This case demonstrates that closer analysis of the qualitative features of fetal movements by, for instance, real-time ultrasound could aid in the antenatal diagnosis of neurologic, particularly convulsive, syndromes. (J Child Neurol 1993;8:164-170).

    Original languageEnglish (US)
    Pages (from-to)164-170
    Number of pages7
    JournalJournal of child neurology
    Volume8
    Issue number2
    DOIs
    StatePublished - Apr 1993

    ASJC Scopus subject areas

    • Pediatrics, Perinatology, and Child Health
    • Clinical Neurology

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