Newborn screening
The Children’s Health℠ Newborn Screening Program, in partnership with the Texas Department of State Health Services, strives to ensure that every baby in Texas receives the benefit of early diagnosis and treatment for the conditions detectable on the state metabolic newborn screen.
What is a newborn screening?
Newborn metabolic screening involves collection of a few drops of blood in order to screen for various treatable conditions. Every baby should be screened initially between 1 and 2 days of age and subsequently between 7 days and 14 days of age.
What are the prep instructions before a newborn screening?
Make the most of your child’s genetics appointment by preparing ahead of time.
The following can be very helpful:
Research your family history - This should include (at minimum) your child’s brothers and sisters, first cousins, aunts and uncles, and grandparents. You will be asked questions at your visit about any history of developmental delay or learning problems, children born with any type of birth defect (such as cleft lip or a heart defect), any women in the family with multiple miscarriages, and any conditions which appear to be running through the family (such as cancer or heart disease at a young age)
Obtain any helpful medical records - If your child has seen a geneticist before, or has had any prior genetic testing, we will need a copy of those medical records and genetic test reports. If any of your family members has had positive genetic testing for a genetic condition, we will need a copy of their genetic test report.
Bring a family photo - This will help the geneticist with his or her physical exam as they examine your child’s facial features.
Newborn screening doctors and providers
- Ralph DeBerardinis, MDPediatric Genetics Specialist
- Markey McNutt, MDPediatric Genetics Specialist
- Luis Umana, MDPediatric Genetics Specialist