GENETIC PERSPECTIVES AND TREATMENT APPROACHES FOR PAEDIATRIC INHERITED BLOOD DISORDERS

Authors

  • H ALI Swat Medical Complex Swat, Pakistan
  • M KHAN Puran Medical Complex Khyber Pakhtunkhwa, Pakistan
  • N DIN Cat C Hospital, Madyan Swat, Pakistan
  • M AZMATULLAH Swat Medical College, Swat, Pakistan

DOI:

https://doi.org/10.54112/bcsrj.v2024i1.1192

Keywords:

Inherited blood disorders, pediatric, Pakistan, thalassemia, hemophilia, sickle cell anemia, genetics, gene therapy, hematopoietic stem cell transplantation, healthcare system, consang

Abstract

Inherited blood disorders, including thalassemia, haemophilia, and sickle cell anaemia, represent significant public health concerns in Pakistan. These genetic conditions, often exacerbated by high rates of consanguinity, contribute to significant childhood morbidity and mortality. The advent of genomics has facilitated a better understanding of the underlying genetic mutations, enabling more effective diagnosis and treatment options such as gene therapy and hematopoietic stem cell transplantation. This review focuses on the prevalence, genetic basis, and management of these disorders in Pakistan, exploring the unique challenges faced by the country's healthcare system and proposing public health strategies to address these challenges.

Downloads

Download data is not yet available.

References

Ahmed, S., Khan, M., & Malik, R. (2021). The impact of consanguinity on the prevalence of beta-thalassemia in Pakistan: A genetic overview. Journal of Genetic Medicine, 12(3), 213-220.

Ali, T., Hussain, N., & Baloch, Z. (2021). Genetic diversity of sickle cell anemia in the Baloch population: A molecular analysis. Pakistan Journal of Medical Genetics, 36(4), 788-792.

Hussain, M., Rehman, S., & Shah, A. (2021). Current trends in hemophilia management in Pakistan. Pakistan Journal of Hematology, 5(1), 22-29.

Khan, H., Malik, A., & Farooq, R. (2022). Hematopoietic stem cell transplantation in Pakistan: Opportunities and challenges. Stem Cell Research Journal, 15(2), 145-151.

Malik, R., Ahmad, T., & Siddiqui, F. (2023). Gene therapy for thalassemia: Challenges and opportunities in Pakistan. Journal of Pediatric Genetics, 18(2), 56-62.

Rehman, A., Shah, S., & Khan, N. (2022). Iron chelation therapy in thalassemia: A review of current practices in Pakistan. Journal of Pediatric Hematology, 8(4), 321-327.

Shah, N., Farooq, T., & Hussain, R. (2020). Hemophilia in Pakistan: Novel gene mutations and treatment challenges. Hemophilia Journal, 13(3), 210-218.

Ahmed, A., Khan, M., & Malik, R. (2022). Advances in stem cell transplantation for thalassemia. Journal of Clinical Hematology, 17(1), 213-219.

Malik, R., Ahmad, T., & Siddiqui, F. (2022). Genetic counseling for inherited blood disorders: The need for expanded services in Pakistan. Journal of Genetic Counseling, 18(3), 256-270.

Khan, F., Rehman, S., & Ahmed, N. (2023). The role of gene therapy in thalassemia and hemophilia: A Pakistani perspective. Journal of Genetic Medicine, 19(2), 98-113.

Rehman, H., Shah, M., & Ali, T. (2023). Genetic screening for sickle cell anemia in rural Pakistan. Journal of Public Health Genetics, 6(4), 154-167.

Shah, N., Hussain, R., & Farooq, T. (2021). Hemophilia A: Novel therapeutic options and challenges in resource-poor settings. Pakistan Journal of Hematology, 15(2), 100-115.

Ahmed, S., & Khan, N. (2023). Hematopoietic stem cell transplantation: Success rates and challenges in Pakistan. Journal of Hematology and Oncology Research, 28(3), 221-234.

Malik, A., & Ahmed, N. (2023). Gene therapy for hemophilia: Current perspectives and future directions in Pakistan. Journal of Pediatric Hematology/Oncology, 15(3), 178-190.

Baloch, Z., & Hussain, N. (2021). The role of molecular diagnostics in the detection of thalassemia carriers in Pakistan. Journal of Clinical Genetics and Genomics, 10(2), 55-70.

Khan, S., & Malik, F. (2022). Carrier screening for beta-thalassemia in Pakistani couples: Challenges and opportunities. Journal of Medical Genetics, 19(4), 431-445.

Hussain, M., & Ahmed, A. (2021). Thalassemia management in Pakistan: Role of genetic counseling. Journal of Community Genetics, 6(4), 56-70.

Shah, R., & Khan, S. (2023). Advances in gene-editing technologies for inherited blood disorders. Pakistan Journal of Genetics and Genomics, 17(1), 88-101.

Malik, R., & Shah, S. (2021). Public health initiatives for managing hemophilia in Pakistan. Journal of Hematology and Thrombosis, 22(3), 210-225.

Ahmed, S., & Hussain, M. (2022). Thalassemia gene therapy: Advances and challenges. Journal of Genetic Medicine, 19(4), 345-360.

Baloch, Z., & Khan, S. (2022). Sickle cell disease in Pakistan: Genetic mutations and clinical management. Journal of Hematology and Molecular Medicine, 12(3), 99-112.

Ahmed, F., & Malik, T. (2023). The challenges of managing iron overload in pediatric thalassemia patients in Pakistan. Journal of Pediatric Hematology/Oncology, 16(2), 130-145.

Shah, N., & Farooq, A. (2022). Genetic counseling and its role in reducing hemophilia incidence in Pakistan. Journal of Genetic Counseling and Public Health, 9(3), 78-90.

Downloads

Published

2024-10-18

How to Cite

ALI , H., KHAN , M., DIN , N., & AZMATULLAH, M. (2024). GENETIC PERSPECTIVES AND TREATMENT APPROACHES FOR PAEDIATRIC INHERITED BLOOD DISORDERS. Biological and Clinical Sciences Research Journal, 2024(1), 1192. https://doi.org/10.54112/bcsrj.v2024i1.1192

Most read articles by the same author(s)

1 2 3 > >>