
pmid: 3933281
handle: 11365/30603
Clinical morphological and biochemical aspects of Familial Progressive Myoclonus Epilepsies are reported, classified into 6 main groups, according to their biochemical pathogenesis: neuronal ceroid lipofuscinosis, Lafora's disease, sialidosis, glycopeptiduria, progressive myoclonus epilepsy Unverricht-Lundborg's type, mitochondrial encephalo-neuro-myopathies. A possible pathogenetic mechanism for all the syndromes is reported.
Neuronal Ceroid-Lipofuscinoses, Glycopeptides, Humans, Epilepsies, Myoclonic
Neuronal Ceroid-Lipofuscinoses, Glycopeptides, Humans, Epilepsies, Myoclonic
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