What is Early Check?

Watch this short video to learn more about Early Check. You can read the text instead of watching the video by clicking the "Read" link.

Key information about Early Check

Early Check uses screening tests, including a test called DNA sequencing to check the genes for health conditions in babies.
If your baby doesn’t have enough sample left after newborn screening to test or the quality of the sample is poor, Early Check will not be able to do the screening. Early Check will notify you if this happens.
Most babies with these conditions do not have a family history of the condition, even though the conditions tested are genetic and can run in families.
Most babies get a normal result. For most parents, once you receive your baby’s normal results, your participation in Early Check is over.
Only a small number of babies will have a result that is not normal. Babies who have these conditions may not have any signs at birth. Symptoms can start later and can be mild or serious.
For many conditions, early diagnosis and treatment before symptoms start makes a big difference for a baby’s health and gives them a better start to life.
If Early Check finds a serious health condition in a baby, the Early Check team will connect the parents to more information and help them find doctors and support for their child.

Joining Early Check is your choice

As a parent, taking part in Early Check is up to you. If parents want Early Check screening for their babies, they must sign up on this website.
You can choose extra groups of health conditions to be screened for your baby.
Babies in North Carolina have standard newborn screening, even if they don’t sign up for Early Check.