Newborn screening tests are a service of the public health department performed daily in each US state. Each newborn is tested for a number of health disorders that are not supposed to be present at ...
Should all babies have their genomes sequenced at birth? The question has been hotly debated for the past 15 years. Unlocking the genome’s 3.2-billion-letter code promises understanding of both health ...
UCSF Pediatrics Professor Jennifer Puck, MD, has spent decades pushing for universal newborn screening to detect severe combined immune deficiency (SCID), a rare but deadly genetic disorder. Today, ...
Plummeting costs of DNA sequencing technologies are injecting urgency into the longstanding debate over whether to dive deeper into the genomes of more infants — even apparently healthy ones. Experts ...
This article is the latest in the Health Affairs Forefront featured topic, “Health Policy at a Crossroads,” produced with the support of the Commonwealth Fund and the Robert Wood Johnson Foundation.
The birth of a baby is a moment of immense joy, but it also brings with it many health considerations, especially for preterm ...
Arizona's newborn screening program is adding two more conditions: Duchenne Muscular Dystrophy and a rare genetic disorder called Krabbe.
Twenty-one families took the state of Minnesota to court, forcingchanges regarding how long the state can keep bloodspots taken from newborns for screening. The families argued that the Minnesota ...
When a baby is born in the United States, a few drops of blood are taken from their heel to test for many conditions that could affect the child’s long-term health or survival. This testing is part of ...
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