Scroll to Top

Volume : XIV, Issue : V, June - 2024

A COMPARTMENTAL MATHEMATICAL MODEL OF SICKLE CELL DISEASE: TRANSMISSION DYNAMICS, EQUILIBRIUM ANALYSIS, AND INTERVENTION STRATEGIES FOR RARE GENETIC DISORDERS

Puspanjali Kumari, None

By : Laxmi Book Publication

Abstract :

Sickle Cell Disease (SCD) is a hereditary blood disorder caused by a genetic mutation in hemoglobin, leading to severe health complications, reduced life expectancy, and socio-economic challenges. Despite being classified as a rare disease globally, SCD remains a significant public health concern in certain regions, particularly where consanguinity and carrier prevalence are high.

Keywords :


Article :


Cite This Article :

Puspanjali Kumari, None(2024). A COMPARTMENTAL MATHEMATICAL MODEL OF SICKLE CELL DISEASE: TRANSMISSION DYNAMICS, EQUILIBRIUM ANALYSIS, AND INTERVENTION STRATEGIES FOR RARE GENETIC DISORDERS. Indian Streams Research Journal, Vol. XIV, Issue. V, http://isrj.org/UploadedData/11326.pdf

References :

  1. Nony, P., Kurbatova, P., Bajard, A., Malik, S., Castellan, C., Chabaud, S., ... & CRESim and Epi-CRESim study groups. (2014). A methodological framework for drug development in rare diseases. Orphanet journal of rare diseases, 9, 1-10.
  2. Pearson, I., Rothwell, B., Olaye, A., & Knight, C. (2018). Economic modelling considerations for rare diseases. Value in Health, 21(5), 515-524.
  3. de Mello, C. P. P., Rumsey, J., Slaughter, V., & Hickman, J. J. (2019). A human-on-a-chip approach to tackling rare diseases. Drug discovery today, 24(11), 2139-2151.

Article Post Production

    No data exists for the row/column.
Creative Commons License
Indian Streams Research Journal by Laxmi Book Publication is licensed under a Creative Commons Attribution 4.0 International License.
Based on a work at http://oldisrj.lbp.world/Default.aspx.
Permissions beyond the scope of this license may be available at http://oldisrj.lbp.world/Default.aspx
Copyright � 2014 Indian Streams Research Journal. All rights reserved
Looking for information? Browse our FAQs, tour our sitemap, or contact ISRJ
Read our Privacy Policy Statement and Plagairism Policy. Use of this site signifies your agreement to the Terms of Use