Copyright: ©Author(s) 2026.
World J Clin Pediatr. Sep 9, 2026; 15(3): 118721
Published online Sep 9, 2026. doi: 10.5409/wjcp.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 |
| M | 67 (63.8) |
| F | 38 (36.2) |
| Sex ratio (M:F) | 1.76:1 |
| Age | |
| Mean (years) ± SD | 6.26 ± 3.96 |
| Range | (5 months-14 years) |
| Consanguinity | 62 (59) |
| Non-consanguinity | 43 (41) |
Table 2 Neurological syndromes by consanguinity status, n (%)
| Syndrome | Consanguineous | Non-consanguineous | Total |
| n | 62 | 43 | 105 |
| Genetic syndromes | 36 (58.1) | 18 (41.9) | 54 (51.4) |
| Brain dysplasia | 4 (6.5) | 6 (14.0) | 10 (9.5) |
| Epilepsy | 47 (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 epilepsy | 47 (75.8) | 33 (76.7) | 80 (76.2) | 0.01 | 0.91 |
| Epilepsy type among epilepsy cases | |||||
| Focal epilepsy | 23 (48.9) | 20 (60.6) | 43 (53.8) | 1.06 | 0.30 |
| Generalized epilepsy | 22 (46.8) | 12 (36.4) | 34 (42.5) | 0.87 | 0.35 |
| Undetermined | 2 (4.3) | 0 (0.0) | 2 (2.5) | 1 | 0.34 |
| Type not documented | 0 (0.0) | 1 (3.0) | 1 (1.3) | 1 | 0.41 |
Table 4 Association between developmental disorders and consanguinity status, n (%)
| Developmental disorder | Consanguineous | Non-consanguineous | Total | χ2 | P value |
| Any developmental disorder | 45 (72.6) | 28 (65.1) | 73 (69.5) | 0.67 | 0.41 |
| GDD/ID | 32 (51.6) | 19 (44.2) | 51 (48.6) | 0.56 | 0.45 |
| Language delay | 11 (17.7) | 6 (14.0) | 17 (16.2) | 0.27 | 0.60 |
| Motor impairment | 17 (27.4) | 6 (14.0) | 23 (21.9) | 2.69 | 0.10 |
| ASD | 2 (3.2) | 2 (4.6) | 4 (3.8) | 1 | 0.36 |
Table 5 Developmental disorders among children with epilepsy, stratified by consanguinity status, n (%)
| Developmental disorder | Epilepsy + consanguineous | Epilepsy + non-consanguineous | Total | χ2 | P value |
| n | 48 | 32 | 80 | ||
| Any developmental disorder | 36 (75.0) | 25 (78.1) | 61 (76.3) | 0.10 | 0.75 |
| GDD/ID | 23 (47.9) | 14 (43.8) | 37 (46.3) | 0.13 | 0.71 |
| Language delay | 7 (14.6) | 4 (12.5) | 11 (13.8) | 0.07 | 0.79 |
| Motor impairment | 11 (22.9) | 3 (9.4) | 14 (17.5) | 2.44 | 0.12 |
| ASD | 2 (4.2) | 0 (0.0) | 2 (2.5) | 1 | 0.36 |
- Citation: Alhamoud AH, Granana NE, Bajahzer MF, Muthaffar AM, Sabi MA, Aboelsoud AA, Harbi RH, Harbi MH, Hawas AM. Association between consanguinity and neurological and developmental disorders in pediatric patients: A retrospective cohort study in Jazan, Saudi Arabia. World J Clin Pediatr 2026; 15(3): 118721
- URL: https://www.wjgnet.com/2219-2808/full/v15/i3/118721.htm
- DOI: https://dx.doi.org/10.5409/wjcp.118721