Spinocerebellar ataxia type 14 (SCA14) is a rare autosomal dominant neurodegenerative disease caused by mutations in protein kinase C gamma gene (PRKCG), encoding the PKCγ protein, leading to a progressive cerebellar atrophy and dysfunction characterized by motor impairments and cognitive decline [4]. The gene discussed is PRKCG; the disease is Cerebellar atrophy.