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Retrospective Cohort Study
Copyright: ©Author(s) 2026.
World J Clin Pediatr. Sep 9, 2026; 15(3): 118721
Published online Sep 9, 2026. doi: 10.5409/wjcp.118721
Table 1 Sociodemographic characteristics of the study population, n (%)
Characteristic
Value
Total participants (n)105
M67 (63.8)
F38 (36.2)
Sex ratio (M:F)1.76:1
Age
    Mean (years) ± SD6.26 ± 3.96
    Range(5 months-14 years)
Consanguinity62 (59)
Non-consanguinity43 (41)
Table 2 Neurological syndromes by consanguinity status, n (%)
Syndrome
Consanguineous
Non-consanguineous
Total
n6243105
Genetic syndromes36 (58.1)18 (41.9)54 (51.4)
Brain dysplasia4 (6.5)6 (14.0)10 (9.5)
Epilepsy47 (75.8)33 (76.7)80 (76.2)
Table 3 Association between epilepsy and consanguinity status, n (%)
Epilepsy
Consanguineous
Non-consanguineous
Total
χ2
P value
Any epilepsy47 (75.8)33 (76.7)80 (76.2)0.010.91
Epilepsy type among epilepsy cases
Focal epilepsy23 (48.9)20 (60.6)43 (53.8)1.060.30
Generalized epilepsy22 (46.8)12 (36.4)34 (42.5)0.870.35
Undetermined2 (4.3)0 (0.0)2 (2.5)10.34
Type not documented0 (0.0)1 (3.0)1 (1.3)10.41
Table 4 Association between developmental disorders and consanguinity status, n (%)
Developmental disorder
Consanguineous
Non-consanguineous
Total
χ2
P value
Any developmental disorder45 (72.6)28 (65.1)73 (69.5)0.670.41
GDD/ID32 (51.6)19 (44.2)51 (48.6)0.560.45
Language delay11 (17.7)6 (14.0)17 (16.2)0.270.60
Motor impairment17 (27.4)6 (14.0)23 (21.9)2.690.10
ASD2 (3.2)2 (4.6)4 (3.8)10.36
Table 5 Developmental disorders among children with epilepsy, stratified by consanguinity status, n (%)
Developmental disorder
Epilepsy + consanguineous
Epilepsy + non-consanguineous
Total
χ2
P value
n483280
Any developmental disorder36 (75.0)25 (78.1)61 (76.3)0.100.75
GDD/ID23 (47.9)14 (43.8)37 (46.3)0.130.71
Language delay7 (14.6)4 (12.5)11 (13.8)0.070.79
Motor impairment11 (22.9)3 (9.4)14 (17.5)2.440.12
ASD2 (4.2)0 (0.0)2 (2.5)10.36


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