Progressive familial myoclonus epilepsy.
H. Rustam, Tarik Hamdi, S Witri
Abstract
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H. Rustam, Tarik Hamdi, S Witri
Abstract
Open-access reader
Seven cases of progressive familial myoclonus epilepsy occurring in three families are presented. The patients were in different stages of the illness. The EEG was abnormal in all. It is suggested that these cases belong clinically to the Lafora bodies group. Nystagmus and optic atrophy, seen in one patient, have not been described previously. Myoclonic jerks did not respond to treatment with diazepam and ethosuximide.
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Seven cases of progressive familial myoclonus epilepsy occurring in three families are presented. The patients were in different stages of the illness. The EEG was abnormal in all. It is suggested that these cases belong clinically to the Lafora bodies group. Nystagmus and optic atrophy, seen in one patient, have not been described previously. Myoclonic jerks did not respond to treatment with diazepam and ethosuximide.
Key concepts: Myoclonus, Myoclonic Jerk, Progressive myoclonus epilepsy, Ethosuximide, Medicine, Clonazepam, Epilepsy, Electroencephalography