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Association between consanguinity and neurological and developmental disorders in pediatric patients: A retrospective
Abdullah H Alhamoud1,2, Nora E Granana3, Mohammed F Bajahzer4
1Department of Pediatric Intensive Care Unit, Jazan General Hospital, Jazan Health Cluster, Jazan 82722, Saudi Arabia.
Insights
Parental consanguinity in Saudi Arabia did not show a significant link to specific childhood epilepsy or developmental disorders in this study. Further research with larger populations is needed to confirm these findings on inherited conditions.
Area of Science:
- Pediatric Neurology
- Clinical Genetics
- Public Health
Background:
- Consanguineous marriage is prevalent in Saudi Arabia, increasing the risk of inherited disorders.
- The specific impact of consanguinity on pediatric neurological and developmental outcomes requires further investigation.
Purpose of the Study:
- To investigate the association between parental consanguinity and neurological/developmental disorders in children in Saudi Arabia's Jazan region.
Main Methods:
- Retrospective cohort study of children under 14 with non-acquired neurological or developmental disorders.
- Categorization based on parental consanguinity (second cousins or closer vs. non-consanguineous).
- Statistical comparison of demographic and clinical data using chi-squared or Fisher's exact tests (P < 0.05).
Main Results:
- 105 children included; 59% had consanguineous parents.
- Epilepsy (76%) and developmental disorders (69.5%) were most common.
- No statistically significant differences in disorder types between consanguineous and non-consanguineous groups were found.
Conclusions:
- This study found no clear association between parental consanguinity and the distribution of epilepsy or developmental disorders.
- Observed minor variations were not statistically significant, possibly due to sample size limitations.
- Larger, broader population studies are recommended to explore potential links between consanguinity and these conditions.
Background:
Consanguineous marriage is common in Saudi Arabia and is associated with an increased risk of inherited disorders. However, its relationship with specific neurological and developmental outcomes in children remains incompletely characterized.
Aim:
To examine the association between parental consanguinity and neurological and developmental disorders among pediatric patients in the Jazan region of Saudi Arabia.
Methods:
This retrospective cohort study reviewed the medical records of children younger than 14 years who were diagnosed with non-acquired neurological or developmental disorders at King Fahad Central Hospital between January 2022 and December 2023. Patients were categorized according to parental consanguinity status (second cousins or closer vs non-consanguineous). Demographic and clinical characteristics were compared using χ 2 or Fisher's exact tests, with a significance threshold of P < 0.05.
Results:
A total of 105 children were included (mean age 6.26 ± 3.96 years; 63.8% male), of whom 59% had consanguineous parents. Epilepsy was the most prevalent diagnosis (76%), and developmental disorders were present in 69.5% of the children. Focal epilepsy was the most common epilepsy subtype, while global developmental delay/intellectual disability were the most frequent developmental disorders. Although minor differences were observed in the distribution of epilepsy types and developmental disorders between the consanguineous and non-consanguineous groups, these differences were not statistically significant.
Conclusion:
No clear association was identified between parental consanguinity and the distribution of epilepsy types or developmental disorders in this cohort. Although minor variations were observed between groups, they did not demonstrate statistically significant trends related to parental relatedness, likely reflecting individual variability and the limited sample size. Larger studies across broader populations are needed to further clarify potential associations.
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