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Severe Myoclonic Epilepsy with Crouch Gait in a 10-year-old Male Child: Single Case Report Study
Abstract: The aim of the present study was to characterize changes in gait dysfunction by patients with severe myoclonic epilepsy (SME). Case description with a 10-year-old male child presented with crouch gait, with signs of pyramidal tract involvement, ataxia, and seizures for 10 years duration. The child, born to non-consanguineously married parents presented with seizures. Birth history was normal; based on the history and examination, a clinical diagnosis of epileptic syndrome …
Published in Research and Reviews: A Journal of Medicine · Vol. 8, Issue 2, 2018 · pp. 1–5 Read article