Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil.

T C GhenoG V FurtadoJ A M SauteK C DonisA M V FontanariV E EmmelJ L PedrosoO BarsottiniC Godeiro-JuniorH van der LindenE Ternes PereiraV P CintraW MarquesR M de CastilhosI AlonsoJ SequeirosM Cornejo-OlivasP MazzettiV B LeottiL B JardimMaria-Luiza Saraiva-Pereiranull null

Published in: European journal of neurology (2017)

The progression rate was slower than in other spinocerebellar ataxias. A consistently recurrent intragenic haplotype was found, suggesting a common ancestry for most, if not all, patients.

Keyphrases

end stage renal disease
newly diagnosed
ejection fraction
chronic kidney disease
peritoneal dialysis
early onset
patient reported