spinocerebellar ataxia 37

An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene.

Signs and symptoms

• Ataxia
• Dysarthria
• Cerebellar atrophy
• Frequent falls
• Unsteady gait
• Dysphagia
• Nystagmus
• Tremor