SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families

Neurodegener Dis. 2017;17(4-5):208-212. doi: 10.1159/000464445. Epub 2017 May 31.


Background: Autosomal recessive cerebellar ataxias (ARCA) are a complex group of neurodegenerative disorders with high clinical and genetic heterogeneity. In most cases, the cerebellar ataxia is not pure, and complicating clinical features such as pyramidal signs or extraneurological features are found.

Objective: To identify the genetic origin of the cerebellar ataxia for 3 consanguineous North African families presenting with ARCA.

Methods: Genome-wide high-density SNP genotyping and whole-exome sequencing were performed followed by Sanger sequencing for mutation confirmation.

Results: Two variants were identified in SLC25A46. Mutations in this gene have been previously associated with Charcot-Marie-Tooth type 2 and optic atrophy. While the previously reported variant p.Arg340Cys seems to be consistently associated with the same clinical features such as childhood onset, optic atrophy, gait and speech difficulties, and wasting of the lower limbs, the patient with the novel mutation p.Trp160Ser did not present with optic atrophy and his ocular abnormalities were limited to nystagmus and saccadic pursuit.

Conclusion: In this study, we report a novel variant (p.Trp160Ser) in SLC25A46 and we broaden the phenotypic spectrum associated with mutations in SLC25A46.

Keywords: Ataxia; Mutation; North Africa; SLC25A46.

MeSH terms

  • Adult
  • Cerebellar Ataxia / diagnostic imaging
  • Cerebellar Ataxia / genetics*
  • Consanguinity
  • DNA Mutational Analysis
  • Family Health
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mitochondrial Proteins / genetics*
  • Mutation / genetics*
  • North America
  • Phosphate Transport Proteins / genetics*


  • Mitochondrial Proteins
  • Phosphate Transport Proteins
  • SLC25A46 protein, human