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Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child
Faruk Incecik1, Ozlem M Hergüner1, Atil Bisgin2
1Division of Child Neurology, Department of Pediatrics, Cukurova University Faculty of Medicine, Adana, Turkey.
Abstract:
Autosomal-recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is caused by mutations of the SACS gene, characterized by late-infantile-onset spastic ataxia and other neurological features. ARSACS has a high prevalence in northeastern Quebec, Canada. Recently, several ARSACS cases have been reported from outside Canada. We report typical clinical and neuroimaging features in a Turkish child, which confirmed genetic diagnosis of ARSACS.
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