具有 KCNA2 遗传变异的幼儿的乙酰唑胺反应性早发性缺失癫痫和共济失调 ; 病例报告。
关键词: Absence seizures Acetazolamide Ataxia Genetic variant KCNA2
Mesh : Humans Child, Preschool Acetazolamide / therapeutic use Epilepsy, Absence / drug therapy genetics Ataxia Kv1.2 Potassium Channel / genetics
来 源: DOI:10.1016/j.seizure.2023.06.013