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Newborn screening
/njˈuːbɔːn skɹˈiːnɪŋ/
/nˈuːbɔːɹn skɹˈiːnɪŋ/Newborn screening
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a program that tests newborns for genetic, metabolic, and congenital disorders shortly after birth to detect and treat conditions early
What is "newborn screening"?
Newborn screening is a set of tests performed on infants shortly after birth to check for certain serious health conditions that may not be obvious at birth. These tests typically involve taking a small blood sample from the baby’s heel, which is then tested for various conditions such as metabolic disorders, genetic conditions, and other diseases that can be treated early. Early identification through newborn screening allows for immediate treatment and action, which can prevent serious health issues or developmental problems later on.
Exempel
Tom's congenital hearing loss was detected shortly after birth during a newborn screening.
