Skip to main content
. 2023 Jul 20;6(7):e2324380. doi: 10.1001/jamanetworkopen.2023.24380

Table 1. Demographic Characteristics and Epilepsy Phenotypes.

Characteristic No. (%) (Nā€‰=ā€‰522)
Sex
Male 269 (51.5)
Female 253 (48.5)
Age at seizure onset
Mean (SD), y 1.2 (1.4)
Neonatal (<1 mo) 20 (3.8)
Infantile (1 to <12 mo) 105 (20.1)
Early childhood (1 to <6 y) 229 (43.9)
School-aged (6 to <14 y) 135 (25.9)
Adolescent (ā‰„14 y) 33 (6.3)
Epilepsy type
DEE 142 (27.2)
Non-DEE
GGE 127 (24.3)
IGE 53 (10.2)
NAFE 152 (29.1)
Combined generalized and focal 48 (9.2)
Epilepsy syndrome diagnoses
Syndromes associated with refractory seizures or developmental comorbidities
Any 118 (22.8)
Infantile epileptic spasms syndrome 46 (8.8)
Lennox-Gastaut syndrome 24 (4.6)
Epilepsy with myoclonic-atonic seizures 11 (2.1)
Epilepsy with eyelid myoclonia 9 (1.7)
Spike-and-wave activation in sleep 7 (1.3)
Landau-Kleffner syndrome 5 (1)
Sleep-related hypermotor epilepsy 4 (0.8)
Myoclonic epilepsy in infancy 4 (0.8)
Dravet syndrome 3 (0.6)
Epilepsy of infancy with migrating focal seizures 2 (0.4)
Febrile infection-related epilepsy syndrome 2 (0.4)
Hemiconvulsion-hemiplegia epilepsy syndrome 1 (0.2)
Syndromes associated with milder prognosis
Any 75 (14.4)
Childhood absence epilepsy 34 (6.5)
Self-limited epilepsy with centrotemporal spikes 16 (3.1)
Juvenile myoclonic epilepsy 14 (2.7)
Juvenile absence epilepsy 3 (0.6)
Self-limited infantile epilepsy 3 (0.6)
Self-limited epilepsy with autonomic seizures 2 (0.4)
Epilepsy with generalized tonic-clonic seizures alone 1 (0.2)
Self-limited focal epilepsy 1 (0.2)
Photosensitive occipital lobe epilepsy 1 (0.2)
Responsive to ASMs (seizure-free) 222 (46.4)
Intellectual disability
None 259 (49.6)
Borderline 74 (14.2)
Mild 79 (15.1)
Moderate 59 (11.3)
Severe 38 (7.3)
Profound 13 (2.5)
Other neurodevelopmental diagnoses
Presence of ASD 75 (14.4)
Presence of ADHD 71 (13.6)

Abbreviations: ADHD, attention deficit hyperactivity disorder; ASD, autism spectrum disorder; ASM, antiseizure medication; DEE, developmental and epileptic encephalopathy; GGE, genetic generalized epilepsy; IGE, idiopathic generalized epilepsy; NAFE, nonacquired focal epilepsy.