Article

Epilepsy as the Symptom of a Spinocerebellar Ataxia 13 in a Patient Presenting with a Mutation in the KCNC3 Gene

2023-04-24

Abstract excerpt

<h4>Background: </h4> The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous Group of neurodegenerative diseases, among which SCAl3 is a rare subtype, and its pathogenic gene is the KCNC3 gene. At present, the incidence of SCA13 is still unclear, and only two cases have been reported in the Chinese population. We report a case of SCA13 with ataxia and epilepsy as the clinical manifestati...

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Literature Corpus work: b1878795-d616-5c77-ac81-5e2dc8ad40c7
DOI: 10.21203/rs.3.rs-2835502/v1

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