Among 179 suspected cases, 100 met criteria for encephalitis, including 34 (34%) confirmed, 58 (58%) probable, and 8 (8%) possible cases. Of these, 39 (39%) were classified as infectious encephalitis, most commonly due to herpes simplex virus (11/39, 28.2%), human parechovirus (8/39, 20.5%), and mycoplasma pneumoniae (5/39, 12.8%). 25 cases (25%) were immune-mediated, most commonly myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD; 10/25, 40%), anti–N-methyl-D-aspartate (NMDA) receptor encephalitis (7/25, 28%), and acute disseminated encephalomyelitis (ADEM; 4/25, 16%). The median age was overall 6 years (interquartile range [IQR], 0-12). Patients with infectious encephalitis were younger (median 0 years [IQR, 0–9.5]), whereas those with autoimmune encephalitis, including anti–NMDA receptor encephalitis and glial fibrillary acidic protein astrocytopathy in our cohort, were older (median 14 years [IQR, 10–16]). 48 (48%) required intubation, 3 (3%) died, and 14 (14%) required intensive inpatient rehabilitation due to moderate-to-severe neurological sequelae.