Get the FAQs about Sickle Cell Disease
Understanding Sickle Cell Disease
Sickle Cell Disease (SCD) is a genetic disease of the red blood cells. It is characterized by painful episodes, lower resistance to infections, organ damage, anemia, joint degeneration, strokes, and other health problems. SCD occurs when a child inherits a hemoglobin gene that sickles from both parents. In this case, the child is born with the disease.
Sickle Cell Trait (SCT) occurs when a child inherits a normal hemoglobin gene and a sickle gene. This results in a carrier of the sickle cell gene. SCT is harmless. The concern about the trait is that this abnormal gene can be passed to a child.
A Person with Sickle Cell Disease has an average of 5.6 more hospital encounters annually with 20% having 11 or more encounters annually.
Hospital encounters for Sickle Cell Disease increased 24% from
In Connecticut, nearly
40,000 people carry the
Sickle Cell Trait.