[Spinocerebellar ataxia type 8 in Russian patients].

Evgenii Nuzhnyi Natalia Y Abramycheva I A Chkhartishvili A O Protopopova E Yu Fedotova Sergey Nikolaevich Illarioshkin

Published in: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova (2022)

SCA8 is a rare form of autosomal dominant ataxia with a predominance of the classical phenotype. All identified cases of SCA8 were sporadic, which should be taken into account when planning genetic testing in patients with spinocerebellar ataxia.

Keyphrases

end stage renal disease
early onset
ejection fraction
newly diagnosed
chronic kidney disease
prognostic factors
late onset
peritoneal dialysis