Saffie P, Kauffman MA, Fernandez JM, Acosta I, Espay AJ, de la Cerda A.; Neurology. 2017 Oct;89(14) e178-e179. doi:10.1212/wnl.0000000000004556. PMID: 28972115.
ARSACS is the second most common cause of autosomal recessive spastic ataxia syndrome (SACS mutations account for 37% of Friedreich-negative cases)1 and should be considered in any population with suggestive MRI abnormalities.
Saturday, November 4, 2017
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