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Browse result for Idiopathic generalized epilepsy

※ introduction

    Idiopathic generalized epilepsy (IGE) is a group of epileptic disorders that are believed to have a strong underlying genetic basis. IGE is considered a subgroup of Genetic Generalized Epilepsy (GGE). Patients with an IGE subtype are typically otherwise normal and have no structural brain abnormalities. People also often have a family history of epilepsy and seem to have a genetically predisposed risk of seizures. IGE tends to manifest itself between early childhood and adolescence although it can be eventually diagnosed later. The genetic cause of some IGE types is known, though inheritance does not always follow a simple monogenic mechanism.

Reference
Wiki: Idiopathic generalized epilepsy



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD02077A6NFN314671
RBFOX3
RNA binding protein fox-1 homolog 3
Homo sapiens
PTMD01380O951808912
CACNA1H
Voltage-dependent T-type calcium channel subunit alpha-1H
Homo sapiens
PTMD02283O00305785
CACNB4
Voltage-dependent L-type calcium channel subunit beta-4
Homo sapiens
PTMD02423O147642563
GABRD
Gamma-aminobutyric acid receptor subunit delta receptor subunit delta)
Homo sapiens