CONGENITAL ABNORMALITIES IN NEWBORNS OF CONSANGUINEOUS AND NON-CONSANGUINEOUS PARENTS
DOI:
https://doi.org/10.54112/pjicm.v5i02.127Keywords:
Congenital Anomalies, Consanguinity, Neonatal Malformations, Genetic Risk, Pakistan, Prenatal CounselingAbstract
Background: Congenital abnormalities contribute significantly to neonatal morbidity and mortality worldwide. Consanguinity is recognized as a potential risk factor for various structural and genetic malformations, yet its impact on the prevalence of specific anomalies in local populations remains underreported. Objective: To determine the frequency of congenital abnormalities in newborns of consanguineous versus non-consanguineous parents. Study Design: Cross-sectional study. Setting: Department of Obstetrics and Gynecology, Saidu Medical College, Swat, Pakistan. Duration of Study: November 1, 2024, to May 1, 2025. Methods: A total of 207 women with fetuses diagnosed with congenital malformations were enrolled. Diagnoses included clubfoot, congenital heart disease, cleft palate, polycystic kidney disease, and anencephaly, confirmed through physical examination and relevant diagnostic tests. Frequencies of anomalies were compared between consanguineous and non-consanguineous groups using the chi-square test, with p-values <0.05 considered statistically significant. Results: The mean maternal age was 27.52 ± 7.80 years. Congenital heart disease was significantly more common among consanguineous cases (17.4%) than non-consanguineous cases (3.6%) (p = 0.001). Similarly, cleft palate occurred in 15.9% vs. 2.9%, polycystic kidney disease in 7.2% vs. 1.4%, and anencephaly in 5.8% vs. 0.7%, respectively. Conclusion: Congenital abnormalities were significantly more frequent among newborns of consanguineous parents compared to those of non-consanguineous parents. These findings highlight the importance of genetic counseling and public health interventions in populations with high rates of consanguineous marriages.
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