Newborn Screening Tests

Newborn Screening Tests

What are newborn screening tests?

The U.S. has a national program of
newborn screening tests to check for several different disorders that can be treated
they are found very early in life. If the “screening” test results are abnormal, it
means further tests need to be done to tell whether the baby has a disorder.  There
is a
core set of 34 newborn screening tests for the entire country. But, additional tests
done vary among the states. Some disorders are more common in some states, making
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’s 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’s caused by a deficiency of an enzyme needed to digest an amino acid called

  • 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) can’t 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’s 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’s 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.