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Newborn Screening Tests

Newborn Screening Tests

What are newborn screening tests?

Picture of a nurse examining a newborn

Nearly all newborns have screening tests to check for several different disorders. They are called screening tests because all newborns get them. And if the test results are abnormal, further tests are done.  The U.S. has a national program with a core set of newborn screening tests. Each state requires screening tests, but the specific 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 many 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 and has almost doubled in the past 20 years. Untreated low thyroid hormone levels can lead to mental 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 begin 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 necessary 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, which helps control energy, sugar levels, blood pressure, and how the body responds to the stress of injury or illness. It is extremely 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. 

Most screenings can't be done until a baby has received at least 24 hours of breast milk or formula. 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: 09-22-2014

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Endocrinology/Diabetology
Dr. Ayanna Butler-Cephas
Dr. Eric Gyuricsko
Dr. Kent Reifschneider
Dr. Reuben Rohn
Dr. Melissa Russell
Dr. Marta Satin-Smith
Health Tips
Earlier is Better to Catch Hearing Loss
Diseases & Conditions
Anatomy of the Newborn Skull
Assessments for Newborn Babies
Baby's Care After Birth
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Breastfeeding: Getting Started
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Chromosomal Abnormalities
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Digestive Disorders in Children
Evaluating a Child for Birth Defects
Fever in A Newborn
Getting Ready at Home
Getting to Know Your New Baby
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Hearing Screening Tests for Newborns
Heart Disorders
High-Risk Newborn Blood Disorders
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Taking Your Baby Home
Testing and Lab Procedures for the Newborn in Intensive Care
The Growing Child: Newborn
The Respiratory System in Babies
Thrush
Transient Tachypnea of the Newborn
Umbilical Cord Care
Vision and Hearing
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Warmth and Temperature Regulation
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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.