Exams and Tests
Sickle cell disease is diagnosed when initial tests show abnormal
hemoglobin, with more testing if needed. A
sickle cell test looks for
sickle cell trait and sickle cell disease.
Prenatal testing
Doctors can diagnose sickle cell
disease before a child is born (prenatally). Couples who are at risk for
passing on this disease to their offspring may want to talk with a
genetic counselor about prenatal testing.
Infant screening
Sickle cell disease can be
diagnosed at birth. Most states in the United States screen all newborns for
sickle cell disease along with other common disorders. You can also request
screening.
Soon after birth, a sample of blood is taken from the
infant's heel and sent to a lab, where it is screened for the presence of
sickle cell hemoglobin (hemoglobin S).
Adult screening
If one member of a couple has
sickle cell disease or sickle cell trait, the other member should be tested
before becoming pregnant. This test requires a blood sample, which is screened
for the presence of hemoglobin S, hemoglobin C, or
beta-thalassemia.
If one or both members
of a couple carry a hemoglobin S
gene or another abnormal hemoglobin gene, the couple
may want to meet with a genetic counselor before becoming pregnant to learn
more about their chances of having a child with sickle cell disease. Your
doctor can help you find a genetic counselor to discuss a
genetic test.
Pulmonary hypertension is a severe, common problem for people with sickle cell
disease. It can be detected early with an
echocardiogram, a painless method of measuring blood
flow. Some experts suggest all adults with sickle cell disease get
screened.1, 3