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Article

Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 gene.

BMC neurology - 26 Jun 2023

Li Shao, Shang Dandan, Du Yanjiao, Li Yan, Liu Ruihua

Abstract excerpt

BACKGROUND: The spinocerebellar ataxias (SCAs) refer to a diverse group of neurodegenerative illnesses that vary clinically and genetically. One of the rare subtypes within this group is SCA13, caused by mutations in the KCNC3 gene. Currently, the prevalence of SCA13 remains uncertain, with only a couple of cases being documented in the Chinese population. This study presented a case study of SCA13, where the...

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Identifiers

PMID: 37365508
DOI: 10.1186/s12883-023-03304-5
PMCID: PMC10294460

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