Adding genomic sequencing to the standard newborn screening heel-prick test is changing how we diagnose kids with genetic ...

September is Newborn Screening Awareness Month, highlighting the importance of early detection and intervention for newborns. Here, Dr. Joshua Baker, attending physician in genetics, genomics and ...

One of the great successes of public health in the US is the newborn screening program, which tests infants in every state for more than 30 serious but treatable congenital diseases. For the four ...

Adding genomic sequencing to newborn blood screening would detect hundreds of additional childhood conditions, providing much ...

The X-linked neuromuscular disorder Duchenne muscular dystrophy (DMD), which historically has been diagnosed in boys between the ages of 3 and 6 years, has become an important candidate for newborn ...

The birth of a baby is a moment of immense joy, but it also brings with it many health considerations, especially for preterm ...

Seven recommendations developed, including use of floating immunoreactive trypsinogen cutoff over fixed cutoff. HealthDay News — In a guideline issued by the US Cystic Fibrosis Foundation and ...

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.

BUFFALO, N.Y. (WIVB) — The Federal Newborn Screening Advisory Committee voted to add Krabbe Leukodystrophy Disease to the recommended newborn screening panel (RUSP), which is a huge victory for Hunter ...

The newborn screening program for early identification of hereditary diseases, one of the most successful public health programs in United States, was introduced more than 60 years ago. As the ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. A little over 40% of parents did not know about the ...