Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare genetic epilepsy syndrome characterized by infantile or childhood onset of focal motor seizures remitting with age, as well as childhood onset of exercise-induced dystonia which often persists into adulthood. Additional reported features include nystagmus and postural tremor of the hands. Disease data Klasyfikacja Disease Synonimy Rolandic epilepsy exercise-induced dystonia Kod ORPHA 163727 Kod OMIM 608105 Kod ICD10 G40.4 Kod ICD11 8A61.2Y *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl