Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare epilepsy syndrome characterized by progressive myoclonus epilepsy in association with primary glomerular disease. Patients present with neurologic symptoms (including tremor, action myoclonus, tonic-clonic seizures, later ataxia and dysarthria) that may precede, occur simultaneously or be followed by renal manifestations including proteinuria that progresses to nephrotic syndrome and end-stage renal disease. In some patients, sensorimotor peripheral neuropathy, sensorineural hearing loss and dilated cardiomyopathy are associated symptoms. Disease data Klasyfikacja Disease Synonimy AMRF EPM4 Postępująca padaczka miokloniczna typu 4 Zespół mioklonii i nefropatii EPM4 Myoclonus-nephropathy syndrome Progressive myoclonic epilepsy type 4 Progressive myoclonus epilepsy type 4 Kod ORPHA 163696 Kod OMIM 254900 Kod ICD10 G40.4 Kod ICD11 - *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