Familial Benign Neonatal Epilepsy

Overview of Familial Benign Neonatal Epilepsy

Most recent studies have shown that Familial Benign Neonatal Epilepsy shares some biological mechanisms with absence-epilepsy, autosomal-dominant-form-of-benign-neonatal-seizures, benign-neonatal-epilepsy, channelopathies, convulsion-neonatal, convulsions, epilepsies-myoclonic, epilepsies-partial, epilepsy, epilepsy-frontal-lobe, epilepsy-generalized, febrile-convulsions, idiopathic-generalized-epilepsy, infantile-severe-myoclonic-epilepsy, infantile-spasms, myoclonic-epilepsy-juvenile, nervousness, partial-seizure, tonic-clonic-epilepsy.

Among the many pathways, these few ones have gauged particular interests from scientists studying Familial Benign Neonatal Epilepsy, and have been seen in publications frequently: Brain Development, Exocytosis, Fatty Acid Oxidation, Hypersensitivity, Localization, Membrane Depolarization, Muscle Contraction, Pathogenesis, Reflex, Regulation Of Action Potential, Response To Ethanol, Skeletal Muscle Contraction, Transport, Vesicle Docking

Quite a number of genes have been found to play important roles in Familial Benign Neonatal Epilepsy, such as ARX, CA1, CHRNA4, CSTB, GABRG2, KCNA1, KCNQ1, KCNQ2, KCNQ3, KCNQ4, KCNQ5, LGI1, PRRT2, PSMC1, RPS4X, RPS4Y1, SCN1A, SCN1B, SCN2A. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Familial Benign Neonatal Epilepsy Related Genes

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Pathways Related to Familial Benign Neonatal Epilepsy

This information is being compiled and will come in a future update

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