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The first time you see your baby, she's already passed her first test: She's in your arms, and she's yours.
Chances are, you already think she's perfect, thank you very much. But the doctors and nurses surrounding you have other criteria, and they are likely going to run a number of routine tests -- some immediately after birth, others sometime before you're both discharged.
Newborn screening takes two forms. There are simple assessments like the APGAR score, and there's testing for various genetic disorders. If you're thinking, "Didn't I get enough testing when I was pregnant?" remember this: Many of the disorders your baby may be screened for at birth are not visible right away. That's why the American Academy of Pediatrics (AAP) recommends a range of metabolic tests (and is pushing for a standardized, nationwide roster of tests).
The March of Dimes believes all newborns should be tested for at least 29 different disorders. The tests your baby will receive depends on what state you live in (download an updated list of state-mandated tests at http://genes-r-us.uthscsa.edu/nbsdisorders.htm), but may include tests for disorders such as phenylketonuria (PKU); sickle-cell anemia; galactosemia; hypothyroidism; and congenital adrenal hypoplasia (CAH).
Here's a quick snapshot of what will happen in the immediate post-birth period:
What you might also be offered:
For more information, go to the website of the National Newborn Screening and Genetics Resource Center.
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