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Baby Testing: 6 Essential Health Screenings for Your Newborn New 2020

Baby Testing: 6 Essential Health Screenings for Your Newborn

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Baby Testing: 6 Essential Health Screenings for Your Newborn

How it’s done: A few drops of blood from your baby’s heel are sent to a lab for analysis. Doctors can perform multiple tests on that tiny sample.

Why your baby needs it: Although relatively rare, metabolic disorders can cause mental retardation, stunted growth, and even death. But if caught early, potential health problems can be prevented and even reversed. Your baby will be screened for anywhere from three to 50 different disorders, depending on which state he’s born in. At the very least, he’ll be screened for phenylketonuria (a condition that makes it impossible for the body to break down certain food substances), galactosemia (an inherited, genetic condition in which the body lacks the enzyme that breaks down a certain sugar), and congenital hypothyroidism (a disease caused by an underactive thyroid gland). But the Department of Health and Human Services is considering a requirement that at least 30 tests be done by all states.

When it’s done: In the first 24 to 48 hours of life.

Side effects: Usually none. Your baby may feel a slight pinch in her heel. The puncture is covered with a bandage.

Source: Parent
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Baby Testing: 6 Essential Health Screenings for Your Newborn

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