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 |