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.
Guazzi, G.C., Federico, A. (1985). Familial progressive myoclonus epilepsies. ACTA NEUROLOGICA, 7(3-4), 219-227.
Familial progressive myoclonus epilepsies
Federico, A.
1985-01-01
Abstract
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.
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https://hdl.handle.net/11365/30603
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