| Journal of Neurology Research, ISSN 1923-2845 print, 1923-2853 online, Open Access |
| Article copyright, the authors; Journal compilation copyright, J Neurol Res and Elmer Press Inc |
| Journal website https://jnr.elmerpub.com |
Review
Volume 16, Number 2, June 2026, pages 67-76
Seizures and Epilepsy in Children With SARS-CoV-2 Infection: Clinical Phenotypes, Mechanisms, and Long-Term Outcomes
Figure

Table
| Clinical presentation | Key clinical features | Recommended diagnostic approach | Prognostic considerations | References |
|---|---|---|---|---|
| CNS: central nervous system; CSF: cerebrospinal fluid; EEG: electroencephalography; MIS-C: multisystem inflammatory syndrome in children; MRI: magnetic resonance imaging; SARS-CoV-2: severe acute respiratory syndrome coronavirus 2. | ||||
| Isolated simple febrile seizure | Generalized, brief (< 15 min), single seizure, rapid return to baseline | No routine EEG or neuroimaging; supportive care | Generally benign; low risk of subsequent epilepsy | [4–6] |
| Complex febrile seizure | Prolonged (> 15 min), focal features, or recurrent seizures within 24 h | Consider EEG and targeted neuroimaging based on clinical context | Slightly increased risk compared with simple febrile seizures; prognosis generally favorable | [4, 5] |
| Afebrile acute symptomatic seizure | New-onset seizure without fever, preserved consciousness between events | EEG and neuroimaging recommended to exclude structural or inflammatory causes | Outcome depends on underlying etiology; low epilepsy risk if no persistent CNS pathology | [3, 7, 9] |
| Persistent altered mental status or encephalopathy | Prolonged confusion, reduced consciousness, behavioral change | EEG, brain MRI, inflammatory markers; consider CSF analysis | Suggests inflammatory or immune-mediated CNS involvement; variable prognosis | [1–3, 9] |
| Status epilepticus | Prolonged or recurrent seizures without recovery | Urgent EEG, neuroimaging, metabolic and infectious workup | Higher morbidity; prognosis depends on etiology and treatment response | [18, 19, 24, 30] |
| Suspected MIS-C with neurological involvement | Seizures with systemic inflammation, shock, or multisystem involvement | Comprehensive evaluation including EEG, MRI, inflammatory markers, and cardiac assessment | Immune-mediated mechanisms predominate; outcome improves with timely immunomodulatory therapy | [1, 2, 28] |
| Suspected autoimmune encephalitis or demyelinating disease | Subacute seizures, encephalopathy, focal deficits | EEG, MRI, CSF studies, and autoimmune antibody testing | Early recognition and treatment associated with improved neurological outcomes | [13–15, 29] |
| Preexisting epilepsy with transient seizure worsening | Temporary increase in seizure frequency during acute illness | Review adherence, identify triggers; no routine escalation if control returns to baseline | Seizure control typically returns to baseline after recovery | [8, 25, 26] |