Abstract
Sickle cell disease is a rare inherited, lifelong blood disorder affecting an estimated 100,000 individuals in the United States (Centers for Disease Control and Prevention. Sickle Cell Disease (SCD). n.d. https://www.cdc.gov/ncbddd/sicklecell/index.html). Red blood cells contain hemoglobin which is responsible for carrying oxygen to the body. The genetic abnormality in sickle cell disease leads to a change in the shape of the red blood cell which results in vaso-occlusion and impaired blood flow. Vaso-occlusion leads to tissue damage and a resulting vasculopathy. Sickle cell disease can manifest with a variety of acute and chronic complications including pain, increased risk of infection, anemia, stroke, and others.
| Original language | English (US) |
|---|---|
| Title of host publication | Clinical Considerations in School-based Health |
| Subtitle of host publication | An Evidence-Based Guide for Physicians, Advanced practice providers and School nurses |
| Publisher | Springer Science+Business Media |
| Pages | 435-441 |
| Number of pages | 7 |
| ISBN (Electronic) | 9783031857652 |
| ISBN (Print) | 9783031857645 |
| DOIs | |
| State | Published - Jan 1 2025 |
All Science Journal Classification (ASJC) codes
- General Medicine