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. 2024 Oct 7;15:1466075. doi: 10.3389/fneur.2024.1466075

Table 1.

The genes in the article and related diseases and treatments of them.

Gene Related disease Treatment
KCNA1 Epilepsy, Episodic Ataxia Type 1, SUDEP carbamazepine, 4-aminopyridine, SUDEP prevention strategies
KCNA2 Epilepsy, Ataxia, Neurodevelopmental Disorders 4-Aminopyridine, ketogenic diet, gene therapy
KCNB1 Developmental and Epileptic Encephalopathy (DEE), Autism Valproic acid, Angiotensin II, neuroprotective therapies
KCNC1 Epileptic Encephalopathy, Myoclonus Epilepsy, Ataxia Small molecule Kv3 activators, pharmacological treatments
KCND2 Autism, Epilepsy, Cortical Malformations Antagonizing miR-324-5p, Saikosaponin A
KCNQ2 Benign Familial Neonatal Epilepsy (BFNE), Encephalopathy Carbamazepine, KCNQ openers like retigabine, cannabidiol, SCR2682
KCNQ3 Benign Familial Neonatal Epilepsy (BFNE), Developmental Delay Similar treatments to KCNQ2, selective channel openers
KCNH1 Epileptic Encephalopathy, Autism Benzodiazepine, phenytoin, valproate
KCNH5 Developmental and Epileptic Encephalopathy (DEE), Autism Valproate, terbutaline