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Newborn Screening Tests

Newborn Screening Tests

What are newborn screening tests?

Picture of a nurse examining a newborn

The U.S. has a national program of newborn screening tests to check for several different disorders that can be treated if they are found very early in life. If the "screening" test results are abnormal, it means further need to be done to tell whether the baby has a disorder.  Their is a core set of 34 of newborn screening tests for the entire country. But, additional tests done vary among the states. Some disorders are more common in some states, making these individual tests more important in those states.

The baby's blood is checked for most of the disorders. A heel-prick is used to sample the baby's blood. The blood is then sent to a state lab for testing. The baby's heel may have some redness at the pricked site, and some babies may have bruising, but this usually disappears in a few days.

Blood tests for newborn screening may include:

  • Phenylketonuria (PKU). PKU is an inherited disease in which the body can't metabolize a protein called phenylalanine. Without treatment, PKU can cause intellectual disability. Newborn screening for PKU is required in all 50 states.

  • Congenital hypothyroidism. This is a condition in which the baby is born with too little thyroid hormone. Hypothyroidism is also quite common. Untreated low thyroid hormone levels can lead to developmental problems and poor growth. All 50 states screen for hypothyroidism.

  • Galactosemia. This is an inherited disorder in which the baby is unable to metabolize galactose, a milk sugar. Without treatment (avoidance of milk), galactosemia can be life threatening. Symptoms may start in the first 2 weeks of life. All states screen for galactosemia.

  • Sickle cell disease. This inherited disorder occurs primarily in African Americans, but may also occur in Hispanics and Native Americans. The disease causes a severe form of anemia. Early diagnosis of sickle cell disease can help lower some of the risks, which include severe infections, blood clots, and stroke.

  • Maple syrup urine disease. This is an inherited disorder that is very common in the Mennonite population. The disorder is caused by an inability of the body to properly process certain parts of protein called amino acids. The name comes from the characteristic odor of maple syrup in the baby's urine caused by the abnormal protein metabolism. If untreated, it is life threatening as early as the first 2 weeks of life. Even with treatment, severe disability and paralysis can occur.

  • Homocystinuria. This inherited disorder affects 1 in 100,000 babies and causes intellectual disability, bone disease, and blood clots. It is caused by a deficiency of an enzyme needed to digest an amino acid called methionine.

  • Biotinidase deficiency. This inherited disorder is characterized by a deficiency of the biotinidase enzyme. This enzyme is important in metabolizing biotin, a B vitamin.

  • Congenital adrenal hyperplasia. Most states screen for this inherited disease of the adrenal glands. Babies born with congenital adrenal hyperplasia (CAH) cannot make enough of the hormone cortisol. Cortisol helps control energy, sugar levels, blood pressure, and how the body responds to the stress of injury or illness. It is very common in a certain group of Eskimos in western Alaska. CAH may also affect the development of the genitals and the hormones of puberty.

  • Medium chain acyl-CoA dehydrogenase deficiency (MCAD). This disorder of fatty acid oxidation can cause sudden death in infancy and serious disabilities in survivors, such as intellectual disability.

  • Cystic fibrosis. This condition causes serious lung and digestive problems. If diagnosed early, treatment can begin.

  • Severe combined immunodeficiency (SCID). Babies with this disorder are unable to fight infection. There is a high rate of death from the condition. If it is diagnosed early, a bone marrow transplant may be done.

Other conditions are screened with different methods including:

  • Hearing loss. Hearing is checked using a special instrument. Nearly all states are currently testing newborns.

  • Critical congenital heart disease. The level of oxygen in the baby's blood is checked with a device called a pulse oximeter.  If the level is lower than expected, the baby may have a heart conditions.

Most heel prick screenings can't be done until a baby has been eating for at least 24 hours because it takes that long for abnormal levels to show up in the blood. The hearing and heart disease tests are also less reliable in the first 24 hours. Your baby may need follow-up testing if you are discharged before this time or the baby is unable to be tested before discharge. Most states mandate a second blood test to be done at 2 weeks of age.

Reviewed Date: 10-01-2016

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Dr. Ayanna Butler-Cephas
Dr. Eric Gyuricsko
Dr. Kent Reifschneider
Dr. Reuben Rohn
Dr. Melissa Russell
Dr. Marta Satin-Smith
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Disclaimer: This information is not intended to substitute or replace the professional medical advice you receive from your child's physician. The content provided on this page is for informational purposes only, and was not designed to diagnose or treat a health problem or disease. Please consult your child's physician with any questions or concerns you may have regarding a medical condition.