Sickle Cell Disease Diagnosis

If you or your child has symptoms of sickle cell disease, your healthcare provider may use a number of tests to diagnose the condition. If your child’s initial newborn screening results show they may have sickle cell disease or trait, further testing can confirm the diagnosis.

Today's Faces of Sickle Cell Disease: Cassandra Trimnell

In 1987, Cassandra Trimnell became the first child in Iowa to be diagnosed with sickle cell disease through the state’s newborn screening program.

Read Cassandra’s story

Blood tests and genetic tests

If you do not know whether you have sickle cell trait or disease, you can get a blood test. Blood tests can determine if your body makes the hemoglobin S protein and how much. Genetic testing can tell if you have one or two copies of the sickle cell gene. Similar tests can also look for other abnormal hemoglobin types. Genetic tests can help confirm a sickle cell disease diagnosis if results from blood tests are not clear. Some people who have sickle cell disease have one copy of the gene for hemoglobin S and another copy of a gene for a different type of faulty hemoglobin that causes diseases such as thalassemia. Genetic testing or blood tests can check for these conditions.

Prenatal screening

Healthcare providers can also diagnose sickle cell disease before a baby is born. One way to diagnose the disease uses a sample of amniotic fluid (the liquid in the sac surrounding a growing embryo). A second way uses a sample taken from the placenta (the organ that attaches the umbilical cord to the womb).

Testing before birth can be done as early as 8 to 10 weeks into the pregnancy. This testing looks for the sickle cell gene instead of the abnormal hemoglobin. However, this testing cannot tell you how serious the symptoms of sickle cell disease will be.

Newborn screening

In newborn screening programs, healthcare providers prick the heel of the newborn and collect drops of blood on a special card. These are used to test for a variety of treatable conditions, including sickle cell disease. A lab tests the hemoglobin in the sample and sends the results to the provider who ordered the test and to your child's healthcare provider. The most used tests are high-performance liquid chromatography, capillary electrophoresis, and isoelectric focusing.

Providers from a special follow-up newborn screening team will contact you directly if your child has sickle cell disease. The providers will then retest your child to confirm the diagnosis. They may also recommend genetic testing.

Newborn screening programs also find out whether your baby has sickle cell trait and is a carrier of the sickle cell gene. If this is the case, genetic counseling will be offered. When a child has sickle cell trait or sickle cell disease, their future siblings or your child's future children may be a carrier of the sickle cell gene.

Newborn Screening Programs

All 50 states have newborn screening programs. As a result, nearly all newborns in the United States are screened for sickle cell disease and other treatable disorders. Many other countries have similar programs.

Learn about newborn screening programs in the United States

Previous

Symptoms

Next

Sickle Cell Trait

Where this page came from

This page was imported from National Heart, Lung, and Blood Institute. Published by the National Heart, Lung, and Blood Institute (NIH) and, as a work of the United States government, in the public domain; its pictures are not copied (many are licensed stock).

Nobody has written it yet — it is the source material at a new address, which is why search engines are asked to skip it and why no one earns from it. It is up for grabs: take it on, and it is yours to rewrite and to earn from.