Autosomal Recessive Spinocerebellar Ataxia 2 (SCAR2) is a neurological disorder characterised by congenital nonprogressive ataxia, delay in language acquisition, persistent dysarthria, strabismus, nystagmus, hypotonia, and mental retardation.
Diseases of the nervous system
Systemic atrophies primarily affecting the central nervous system
Autosomal recessive
9q34.3
Autosomal Recessive Spinocerebellar Ataxia 2 (SCAR2) is a neurological disorder characterised by congenital nonprogressive ataxia, delay in language acquisition, persistent dysarthria, strabismus, nystagmus, hypotonia, and mental retardation.