EntityQ163905· pop 7· linked from 141 articlesLafora diseaseSign in to savetype of rare, inherited, severe, progressive myoclonic epilepsyConnectionsadolescenceEntityelectroencephalographyEntitymultiple system atrophyEntitydominanceEntitytonic–clonic seizureEntityMERRF syndromeEntityfocal epilepsyEntityUnverricht-Lundborg syndromeEntitygeneralized epilepsyEntityjuvenile myoclonic epilepsyEntityheartEntitychildEntityMiddle EastConceptcellEntityliverEntityskinEntitymedicationEntityInternational Standard Book NumberEntitymuscleEntityAlzheimer's diseaseEntityCategoriesAutosomal recessive disordersDiseases named after discoverersEpilepsy typesNeurological disordersRare diseasesSkin conditions resulting from errors in metabolism