Paper Contents
Abstract
Disease of sickle cells A significant portion of the American population suffers from sickle cell disease (SCD), a group of hereditary blood diseases. Hb S, an aberrant form of hemoglobin, polymerizes when deoxygenated in people with sickle cell disease (SCD), giving their red blood cells a sickle-like shape. Anemia, vascular occlusive discomfort, infections, acute chest syndrome, and other consequences increase the morbidity and mortality risk for those with sickle cell disease. Public health must take into account SCD and its consequences while preserving the health of impacted patients
Copyright
Copyright © 2024 Gaurav kumar kushwaha . This is an open access article distributed under the Creative Commons Attribution License.
Paper ID:
IJPREMS41200028036
ISSN:
2321-9653
Publisher:
ijprems