Sickle Cell Test
Test Overview
A sickle cell test is a blood test done to check for sickle cell trait or sickle cell disease. Sickle cell disease is an inherited blood disease that causes red blood cells to be deformed (sickle-shaped, Opens dialog). The red blood cells deform because they contain an abnormal type of hemoglobin, called hemoglobin S, instead of the normal hemoglobin, called hemoglobin A.
The best way to check for sickle cell trait or sickle cell disease is to look at the blood using a method called high-performance liquid chromatography (HPLC). This test identifies which type of hemoglobin is present. To confirm the results of HPLC, a genetic test may be done.
A person inherits two sets of genes, Opens dialog (one set from each parent). As a result, a person may have:
- Two sets of genes that make normal hemoglobin (hemoglobin A). These people have normal red blood cells unless they have some other blood disease.
- One set of genes that makes hemoglobin A and one set that makes hemoglobin S. These people carry the sickle cell trait (and are called "carriers, Opens dialog"), but they do not have sickle cell disease. Sickle cell trait is usually a harmless condition.
- Two sets of genes that make hemoglobin S. These people have sickle cell disease. Both parents either carry the sickle cell trait or have the disease. Sickled red blood cells often cause recurring health problems.
- One set of genes that makes hemoglobin S and one set that makes some other abnormal type of hemoglobin. Depending on the other type of abnormal hemoglobin, these people may have mild or severe sickle cell disorder.
The United States Preventive Services Task Force recommends that all newborns be tested for sickle cell disease.
