Structural brain changes and disease staging in Friedrich’s ataxia


  • Analysis of MRI volumetrics from patients with Friedrich’s ataxia (FRDA) showed progressive neuroanatomical changes in the cerebellum and spinal cord.

Why this matters

  • FRDA is a rare, hereditary neurological disease involving progressive movement incoordination. There are currently no disease-modifying treatments available.

  • These data provide further insight into the structural brain alterations that occur in this rare disease and may help guide further research and clinical trial design.