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Article

Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients.

Movement disorders : official journal of the Movement Disorder Society - 15 Dec 2010

Teive Hélio A G, Munhoz Renato P, Raskin Salmo, Arruda Walter O, de Paola Luciano, Werneck Lineu C, Ashizawa Tetsuo

Abstract excerpt

Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder caused by an ATTCT repeat intronic expansion in the SCA10 gene. SCA 10 has been reported in Mexican, Brazilian, Argentinean and Venezuelan families. Its phenotype is overall characterized by cerebellar ataxia and epilepsy. Interestingly, Brazilian patients reported so far showed pure cerebellar ataxia, without epilepsy. Here, authors provide...

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Identifiers

PMID: 20818609
DOI: 10.1002/mds.23324
PMCID: PMC3000879

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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