Generalized epilepsy with febrile seizures plus Generalized epilepsy with febrile seizures plus (GEFS+) is a syndromic autosomal dominant disorder where
9 RegisterLog in Sign up with one click: Facebook Twitter Google Share on Facebook generalized Dictionary Thesaurus Idioms Encyclopedia Wikipedia gen·er·al·ized (jen'ĕr-ăl-īzd), Involving the whole of an organ, as opposed to a focal or regional process. ...
Pathogenic variants inSLC2A1, which encodes glucose transporter type 1 (GLUT1), are present in 10% of children with absence epilepsy that has onset before age 4 years; genetic testing should be considered for all children this young with primarily absence seizures.20Chromosomal microarray may also...
The most important and most common subtypes of idiopathic generalized epilepsies (IGE) are childhood and juvenile absence epilepsies (CAE, JAE), juvenile myoclonic epilepsy (JME), and epilepsy with grand mal (generalized tonic-clonic) seizures on awakening (EGMA); closely related are early onset ...
Fig. 1.Clinical differences and areas of overlap within GGE, between IGEs and generalized DEEs. CAE: childhood absence epilepsy, DEE: developmental and epileptic encephalopathy, GTCA: generalized tonic-clonic seizures alone, IGE: idiopathic generalized epilepsy, JAE: juvenile absence epilepsy, JME: ju...
recommended classification system first classifies seizures by location (local, generalized, or unknown); then by type of epilepsy disease (focal, generalized, combined, or unknown); and finally, if the seizure and epilepsy type are part of an overall epilepsy syndrome (eg, JME, CAE, JAE).[4...
general systems framework and theory of goal attainment general transduction general tuberculosis general visceral afferent column general visceral efferent column general-adaptation syndrome generalisability generalised epilepsy with febrile seizures plus, type 3 ...
Fan et al. perform trio-based whole exome sequencing in a cohort of individuals with idiopathic generalized epilepsy, and identify five variants in USP25 i
ContextMultiple studies have reported an overgrowth in head circumference (HC) in the first year of life in autism. However, it is unclear whether this
Epilepsy is associated with genetic risk factors and cortico-subcortical network alterations, but associations between neurobiological mechanisms and macroscale connectomics remain unclear. This multisite ENIGMA-Epilepsy study examined whole-brain struct