Spinocerebellar Ataxia 26 (SCA26)

Spinocerebellar Ataxia 26, also known as spinocerebellar ataxia type 26, is related to spinocerebellar ataxia, autosomal recessive 26 and autosomal dominant cerebellar ataxia type iii, and has symptoms including cerebellar ataxia, ataxia, truncal and gait ataxia. An important gene associated with Spinocerebellar Ataxia 26 is EEF2 (Eukaryotic Translation Elongation Factor 2), and among its related pathways/superpathways are Translational Control and Platelet homeostasis. Affiliated tissues include spinal cord and cerebellum, and related phenotypes are dysarthria and progressive gait ataxia