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Copyright: ©Author(s) 2026.
World J Clin Pediatr. Sep 9, 2026; 15(3): 119877
Published online Sep 9, 2026. doi: 10.5409/wjcp.v15.i3.119877
Table 2 Current literature review snapshot
Domain
Key finding
Ref.
Level of evidence
NosologyOccipital syndromes are formally categorized as SeLEAS (autonomic), COVE (visual), and POLE (photosensitive) within SeLFESpecchio et al[15]; Wirrell et al[20]V (ILAE guidelines)
Prognosis: Self-limitedHigh remission rates by puberty; however, “self-limited” does not equate to “benign”-deficits in attention, language, and visuospatial processing are documented in a substantial minority. (pediatric-specific data)Özkul et al[3]; Wirrell et al[20]IIb (cohort)
Prognosis: StructuralCharacterized by earlier onset, higher risk of intellectual disability, and pharmacoresistance. Lower remission rates, strong correlation with MRI-detected lesions. (pediatric-specific data)Taylor et al[5]; Specchio et al[15]; Bartolini et al[21]IIb (cohort)
NeurocognitionDeficits in executive functioning, visuo-spatial memory, and language are prevalent, particularly if seizure onset occurs before age 5 years. (pediatric data; limited by small sample sizes)Specchio et al[15]; Traianou et al[47]IIb-V
Emerging imagingMEG and FDG-PET improve localization in MRI-negative refractory cases. 7T MRI detects lesions invisible at 1.5T/3T in up to 65% of previously MRI-negative patients (mostly adult/mixed cohorts; pediatric data extrapolated)Carrette and Stefan[22]; Bacon et al[23]; Feldman et al[24]IIa-IIb
SurgeryLesionectomy/topectomy yields 69% Engel Class I seizure freedom in structural OLE at 80 months. Visual field deficits occur in 42% postoperatively (adult/mixed cohorts; pediatric data limited)Detchou and Barrie[25]; Jobst et al[27]; Binder et al[44]IIb (surgical cohort)


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