Abstract
SUMMARY: We present findings on MR imaging in 5 patients with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). In the literature, early atrophy of the superior vermis as well as progressive atrophy of the cerebellar hemispheres and cervical cord was described. We found linear hypointensity on T2 and T2 fluid-attenuated inversion recovery–weighted images in the pons in all of our 5 patients.
- Copyright © American Society of Neuroradiology
In this issue
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay: A Report of MR Imaging in 5 Patients
Jump to section
Related Articles
Cited By...
- Assessment of Whole-Brain White Matter by DTI in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
- The ARSACS phenotype can include supranuclear gaze palsy and skin lipofuscin deposits
- Reviewing the genetic causes of spastic-ataxias
- Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)
- Autosomal recessive cerebellar ataxias: the current state of affairs
- Mutations in SACS cause atypical and late-onset forms of ARSACS
- Autosomal recessive spastic ataxia of Charlevoix-Saguenay