Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition An extremely rare, autosomal recessive, hereditary cerebellar ataxia disorder characterized by early onset of progressive, mild to moderate gait and limb ataxia, moderate to severe dysarthria, and nystagmus or saccadic pursuit, frequently associated with epilepsy, moderate intellectual disability, delayed speech acquisition, and hyporeflexia in the upper extremities. Hyperreflexia in the lower extremities may also be associated. Disease data Classification Disease Synonyms Autosomal recessive spinocerebellar ataxia type 15 Autosomalna recesywna ataksja rdzeniowo-móżdżkowa typu 15 SCAR15 SCAR15 Salih ataxia ORPHA code 404499 OMIM code 615705 ICD10 code G11.1 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