Related Experiment Video
Updated: Mar 27, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Learning About Sickle Cell: The Patient in Early Sickle Cell Disease Case Reports, 1910-1933
1Department of Bioethics and Interdisciplinary Studies, The Brody School of Medicine at East Carolina University, Greenville, NC.
Abstract:
Case reports of sickle cell disease (SCD) from its discovery in 1910 to 1933 provide glimpses into the disease's impact on patients and families. Attending physicians, trying to understand the pathophysiology of and treatments for this newly recognized disease, reported also on the effect of SCD on patients' ability to attend school, play, and work, the kinds and severity of the pain patients endured, the late onset of puberty and slowed development of secondary sex characteristics, and the ways families dealt with loved ones who had the disease. These anonymous patients and families helped "teach" physicians about SCD in the early years after its discovery. The current study uses information gleaned from the third published article in 1915 to 1933.
Related Concept Videos
Multiple Allele Traits
iPS Cell Differentiation
EPS and iPS Cells in Disease Research
Endocarditis II: Clinical Features of Infective Endocarditis
Disorders of Erythrocytes
Erythrocyte disorders can be broadly categorized into two main types: anemic and polycythemic conditions.
A low oxygen-carrying capacity of the blood due to the loss, lower production, or destruction of erythrocytes is termed anemia. Hemorrhagic anemia, for example, occurs when bleeding from an external wound or internal ulcer reduces erythrocyte counts.
On the other...
Bone Marrow Sampling and Transplants
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy...

