Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare, genetic, infantile epilepsy syndrome disease characterized by neonatal- to infancy-onset myoclonic focal seizures occurring in various members of a family, associated in some with mild dysarthria, ataxia and borderline-to-moderate intellectual disability. Disease data Classification Disease Synonyms FIME FIME Familial infantile myoclonus epilepsy ORPHA code 352582 OMIM code 605021 ICD10 code G40.3 ICD11 code - *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