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 ...
Today, the GUARDIAN study is moving newborn screening to genomic sequencing, potentially detecting hundreds of conditions before symptoms even appear. But can this cutting-edge technology replace ...
U.K. health officials are facing pressure to rethink how they expand the list of diseases that all newborns are screened for ...
Researchers at UC San Francisco have found that newborns with an unusual pattern of metabolites in their blood — the byproducts created when the body processes energy — were far more likely to die ...
Stanford AI can predict with over 85% accuracy which premature babies will suffer serious medical complications.
The Generation Study, which is now available at Nottingham University Hospitals (NUH) NHS Trust, tests for more than 200 rare ...
Ranging from heel prick blood tests to hearing and heart screenings, these critical health checks in the first year of a baby ...
Dr. James Gibson and his genetics clinic at Dell Children's Medical Center are expecting a first any day now: The first baby with a lysosomal storage disorder to come to the clinic for treatment ...
TEXAS, USA — The Texas Department of State Health Services (DSHS) announced Wednesday that four additional tests for rare genetic conditions will be added to the state’s newborn screening program.
The mother of a four-year-old boy with a rare muscle disease says screening newborn babies for the condition could "save lives". Amy, 37, from Henleaze in Bristol, said early detection of spinal ...
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