K Knowledge and Perceptions of Female University Students as Prospective Mothers Regarding the Presence of Genetic Disorders in Families

Authors

  • Mirfat Department of Biology, Faculty of Medicine, YARSI University, Indonesia
  • Elyas UIN Mahmud Yunus Batusangkar Sumatera Barat, Indonesia

DOI:

https://doi.org/10.55681/ijssh.v4i3.4236

Keywords:

Genetic Disorders, Knowledge, Perception, Female University Students, Prospective Mothers, Health Education, Genetic Counseling

Abstract

Genetic disorders may have medical, psychological, and social implications for families, particularly prospective mothers at risk of transmitting hereditary conditions. This study aimed to assess knowledge and perceptions of genetic disorders among female university students and examine differences between health-related and non-health-related educational backgrounds. An analytical cross-sectional study was conducted among 114 female students at YARSI University, selected through stratified random sampling by academic year. Participants comprised 75 students from health-related programmes and 39 from non-health-related programmes. Data were analysed using the Pearson chi-square test. The findings showed that 94.7% of health-related students understood the definition of genetic disorders, compared with 71.8% of non-health-related students. Knowledge of heredity as a contributing factor was reported by 93.3% and 89.7%, respectively. However, awareness of specialised healthcare facilities remained limited in both groups, with 85.3% of health-related students and 79.5% of non-health-related students reporting insufficient awareness. A statistically significant difference was identified in knowledge between the two groups, whereas perceptions did not differ significantly. These findings highlight the importance of strengthening genetic health education and awareness of specialised services among female university students.

References

Alotaibi, M. (2024). Parental genetic knowledge and attitudes toward childhood with genetic disorders. Frontiers in Genetics, 15, 1434322.

Bull, L. J., Eslick, G. D., Teutsch, S. M., & Elliott, E. J. (2025). Assessing psychological harms on parents and primary caregivers of children living with a rare disease: A systematic review of the scope and validity of surveys utilized. Clinical Child and Family Psychology Review, 28(3), 612–630.

Centers for Disease Control and Prevention. (2024). Living with Down syndrome. U.S. Department of Health and Human Services.

Centers for Disease Control and Prevention. (2025a). About hemophilia. U.S. Department of Health and Human Services.

Centers for Disease Control and Prevention. (2025b). Autism spectrum disorder (ASD): Causes and risk factors. U.S. Department of Health and Human Services.

Crellin, E., Martyn, M., McClaren, B., & Gaff, C. (2023). What matters to parents? A scoping review of parents' service experiences and needs regarding genetic testing for rare diseases. European Journal of Human Genetics, 31(8), 869–878.

Hermanto, I., Chandra, C. K., Utari, A., Winarni, T. I., & Cayami, F. K. (2024). Knowledge of genetics and attitudes toward genetic testing among university students in Indonesia. Journal of Community Genetics, 15, 433–447.

Jameson, J. L., & Kopp, P. (2022). Principles of human genetics. In J. Loscalzo, A. S. Fauci, D. L. Kasper, S. L. Hauser, D. L. Longo, J. L. Jameson, & J. B. editors (Eds.), Harrison's principles of internal medicine (21st ed.). McGraw Hill.

Kementerian Kesehatan Republik Indonesia. (2023). Cegah thalassemia, hindari pernikahan sesama pembawa sifat. Kementerian Kesehatan Republik Indonesia.

Orsmond, G. I., & Seltzer, M. M. (2007). Siblings of individuals with autism spectrum disorders across the life course. Mental Retardation and Developmental Disabilities Research Reviews, 13(4), 313–320.

RSUP Nasional Dr. Cipto Mangunkusumo. (2026). Layanan rawat jalan. RSUP Nasional Dr. Cipto Mangunkusumo.

Urry, L. A., Cain, M. L., Wasserman, S. A., Minorsky, P. V., & Orr, R. B. (2021). Campbell biology (12th ed.). Pearson.

Witt, S., Schuett, K., Wiegand-Grefe, S., Boettcher, J., & Quitmann, J. (2023). Living with a rare disease—Experiences and needs in pediatric patients and their parents. Orphanet Journal of Rare Diseases, 18, 242.

World Health Organization. (2023). Deferasirox and deferoxamine: Application for inclusion in the WHO Model List of Essential Medicines. World Health Organization.

World Health Organization. (2025). Autism. World Health Organization.

Downloads

Published

2026-10-31

How to Cite

Mirfat, & Elyas. (2026). K Knowledge and Perceptions of Female University Students as Prospective Mothers Regarding the Presence of Genetic Disorders in Families. International Journal of Social Sciences and Humanities, 4(3), 1419–1427. https://doi.org/10.55681/ijssh.v4i3.4236