Ontology highlight
ABSTRACT:
SUBMITTER: Hajnsek S
PROVIDER: S-EPMC4150640 | biostudies-literature | 2013
REPOSITORIES: biostudies-literature
Hajnsek Sanja S Petelin Gadze Zeljka Z Borovecki Fran F Nankovic Sibila S Mrak Goran G Gotovac Kristina K Sulentic Vlatko V Kovacevic Ivana I Bujan Kovac Andreja A
Epilepsy & behavior case reports 20130927
<h4>Introduction</h4>Lafora body disease (LBD) is a rare autosomal recessive disorder characterized by progression to inexorable dementia and frequent occipital seizures, in addition to myoclonus and generalized tonic-clonic seizures (GTCSs). It belongs to the group of progressive myoclonus epilepsies (PMEs), rare inherited neurodegenerative diseases with great clinical and genetic differences, as well as poor prognosis. Since those patients have a pharmacoresistant disease, an adjunctive treatm ...[more]