Behr Syndrome

Abstract

in this article, a 31 year old man with Behr syndrome is presented. Behr syndrome isa rarely described, slow progressive spinocerebellar degeneration and associated with early-onset autosomal recessive hereditary ataxias. The main clinical features are mentol retardation, optic atrophy, cerebellar ataxia and spastic paraparesis. Other neurologic signs can be combined.