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- W4284713426 abstract "The voltage-gated Kv10.2 potassium channel, encoded by KCNH5, is broadly expressed in mammalian tissues, including the brain. Its potential mechanism remains unclear. According to previous studies, dysfunction of Kv10.2 may be associated with epileptic encephalopathies and autism spectrum disorder (ASD). To date, only one disease-causing mutation of KCNH5 has been reported, and it involves a case that presented with seizures and autism symptoms. In this study, we discovered and characterized three de novo mutations in KCNH5 that potentially caused severe conditions observed in three Chinese children. All of them experienced seizures, two of them presented with epileptic encephalopathy, one of them presented with ASD, and one did not relapse after drug withdrawal. Notably, treatment with antiepileptic drugs (AEDs) was effective in all patients whose epileptic seizures were controlled. The structures of the proteins resulting from the mutations were predicted in two of the three cases. This provides powerful insight into clinical heterogeneity and genotype - phenotype correlation in KCNH5-related diseases." @default.
- W4284713426 created "2022-07-08" @default.
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- W4284713426 date "2022-07-07" @default.
- W4284713426 modified "2023-10-14" @default.
- W4284713426 title "Clinical Feature, Treatment, and KCNH5 Mutations in Epilepsy" @default.
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- W4284713426 doi "https://doi.org/10.3389/fped.2022.858008" @default.
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