EPILEPSY IN THE CONSANGUINEOUS FAMILIES AT TRIBAL SOCIETY OF KHYBER PAKHTUNKHWA-PAKISTAN
DOI:
https://doi.org/10.52764/jms.22.30.1.7Keywords:
Consanguinity, Epilepsy, Tribal society, PakistanAbstract
Consanguineous marriages are practiced worldwide but very common as social characteristic norms of the tribal society of Pakistan and have reached (~63%). Couples are married within the blood relatives, inheriting different genetic disorders including epilepsy in their offspring.
Objectives: The present work is the ever first attempt to reaffirm the association between epilepsy disease (ED) and consanguinity in the Tribal Society of Khyber Pakhtunkhwa-Pakistan.
Methodology: Approximately, 150 clinically diagnosed epileptic patients of consanguineous families aging around 20 years were included. Children in this study were aging 7-10 years and male to female ratio among the patients was 1:1.5. The target familial cases were included based on sex, age, parental consanguinity, seizure type, cause of epilepsy, and family history. The parents were interviewed to collect the required information after informed consent. Non-consanguineous families, patients with acquired causes, and those who were not willingly participated were excluded from the study.
Results: Statistical analysis while applying Odds Ratio (OR), Z-test, and Chi-Square, showed significant findings (P< 0.01). For the first and second-degree cousins, the Odds Ratio and its 95% confidence interval (CI) were done. In the current study, the consanguinity in parents of epileptic patients was compared with the general population. Generally, 56 (37.33%) of the patient’s parents were first cousins with (OR=3.245 and 95%-CI=2.26-4.645 and P<0.0001), 24 (16.00%) were second-degree cousins with (OR=3.269 and 95%-CI=2.032-5.258 and P<0.0001) and 70 (46.66%) were unrelated.
Conclusion: The overall consanguinity parentage with (OR=3.252 and 95%-CI=2.345-4.510 and P<0.0001) clearly indicates the potential role of heritage lineage/consanguinity in epilepsy within the consanguineous families.
The present statistical study supports genetic counseling before marriages. More significant genotype-phenotype correlation is also needed to minimize the risk of epilepsy disease.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2022 Journal of Medical Sciences

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
All articles published in the Journal of Medical Sciences (JMS) are licensed under the Creative Commons Attribution 4.0 International License (CC-BY 4.0). Under the CC BY 4.0 license, author(s) retain the ownership of the copyright publishing rights without restrictions for their content, and allow others to copy, use, print, share, modify, and distribute the content of the article even for commercial purposes as long as the original authors and the journal are properly cited. No permission is required from the author/s or the publishers for this purpose. Appropriate attribution can be provided by simply citing the original article. The corresponding author has the right to grant on behalf of all authors, a worldwide license to JMS and its licensees in all forms, formats, and media (whether known now or created in the future), The corresponding author must certify and warrant the authorship and proprietorship and should declare that he/she has not granted or assigned any of the article’s rights to any other person or body.
The corresponding author must compensate the journal for any costs, expenses, or damages that the JMS may incur as a result of any breach of these warranties including any intentional or unintentional errors, omissions, copyright issues, or plagiarism. The editorial office must be notified upon submission if an article contains materials like text, pictures, tables, or graphs from other copyrighted sources. The JMS reserves the right to remove any images, figures, tables, or other content, from any article, whether before or after publication, if concerns are raised about copyright, license, or permissions and the authors are unable to provide documentation confirming that appropriate permissions were obtained for publication of the content in question.

