Progressive Ataxia due to de novo Missense Variants in the CACNA1A Gene

Abstract

The CACNA1A gene encodes the alpha-1A subunit of P/Q type voltage-gated calcium channel Ca_v2.1, which is associated with a broad clinical spectrum and variable symptomatology. While few patients with progressive ataxia caused by CACNA1A missense variants have been reported, here we report three unrelated Chinese patients with progressive ataxia due to de novo missense variants in the CACNA1A gene, including a novel pathogenic variant (c.4999C > G) and a previously reported pathogenic variant (c.4037G > A). Our findings and a systematic literature review show the unique phenotype of progressive ataxia caused by missense variants and enlarge the genetic and clinical spectrum of CACNA1A. This suggests that in addition to routine screening for dynamic mutations, screening for CACNA1A variants is important for clinicians facing patients with progressive ataxia.

Keywords: CACNA1A; De novo; Missense variant; Progressive ataxia.