Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): typical clinical and neuroimaging features in a Brazilian family

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disorder characterized by late-infantile onset spastic ataxia and other neurological features. ARSACS has a high prevalence in northeastern Quebec, Canada. Several ARSACS cases have been reported outside Canada...

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Veröffentlicht in:Arquivos de neuro-psiquiatria 2011, Vol.69 (2B), p.288-291
Hauptverfasser: Pedroso, José Luiz, Braga-Neto, Pedro, Abrahão, Agessandro, Rivero, René Leandro Magalhães, Abdalla, Carolina, Abdala, Nitamar, Barsottini, Orlando Graziani Povoas
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Sprache:eng
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Zusammenfassung:Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disorder characterized by late-infantile onset spastic ataxia and other neurological features. ARSACS has a high prevalence in northeastern Quebec, Canada. Several ARSACS cases have been reported outside Canada in recent decades. This is the first report of typical clinical and neuroimaging features in a Brazilian family with probable diagnosis of ARSACS.
ISSN:0004-282X
1678-4227
1678-4227
0004-282X
DOI:10.1590/S0004-282X2011000300004