Columnist Oluwatosin Adesoye, a doctor, sorts through the difference between sickle cell anemia and sickle cell disease — and ...

Sickle cell disease is caused by mutations in the beta-hemoglobin gene (HBB). Individuals having identical pairs of genes for the HBB glu6val mutation (HbS) have sickle cell anemia; individuals ...

Sickle cell trait evolved as protection against malaria, especially in tropical regions. Its discovery advanced understanding of genetic inheritance, but racial bias long hindered care for affected ...

In the two leading disorders caused by HBB mutations, sickle cell anemia and beta thalassemia, red blood cells can't effectively carry oxygen.

Sickle cell anemia, or sickle cell disease (SCD), is a genetic disease of the red blood cells (RBCs). Normally, RBCs are shaped like discs, which gives them the flexibility to travel through even ...

People with sickle cell anemia are at a higher risk of health problems that impact the heart, lungs, kidneys, and other vital organs because they’re not receiving enough oxygen-filled blood.

Child sickle cell anemia occurs when a child has a lower level of healthy red blood cells than expected. The condition is present from birth, though symptoms do not appear in early infancy.

Currently, the only way to cure sickle cell anemia is by replacing a person’s bone marrow with bone marrow from a donor who is a close genetic match. However, not everyone has a well-matched donor.

Sickle cell anemia (SCA) in infants is a genetic blood disorder. Early identification, appropriate treatment, and regular monitoring can help infants with SCA.

Sickle cell anemia is an inherited disease in which red blood cells are unable to properly carry oxygen throughout the body because of their distinctive crescent-like, or sickle, shape. The ...