Congenital CMV is the most common nongenetic cause of hearing loss in children and a leading cause of other neurologic ...
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 ...
February is Rare Disease month, and two Utah families are leading the way in newborn screening for Creatine Deficiency.
If you have ever welcomed a new baby into the world, you know the mix of hope and uncertainty that comes with those first days. For decades, newborn screening has been a quiet triumph of public health ...
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 ...
The earlier diseases are diagnosed, the earlier they can be treated. Unfortunately, time is often of the essence for those with rare genetic disorders. For example, the few therapies that exist for ...
U.K. health officials are facing pressure to rethink how they expand the list of diseases that all newborns are screened for ...
Early results from a study of newborn screening methods show that DNA analysis picks up many more preventable or treatable serious health conditions than standard newborn screening and is favored by ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. A little over 40% of parents did not know about the ...
An updated report on cystic fibrosis (CF) from Ann & Robert H. Lurie Children's Hospital of Chicago, in partnership with the ...
Isaac has permanent hearing loss in both ears and his deafness was picked up soon after birth, thanks to a newborn hearing ...
There are plans to add two more genetic disorders for screening for Wisconsin’s newborn screening program. X-Linked Adrenoleukodystrophy (X-ALD) and Mucopolysaccharidosis Type 1 (MPS 1) will be part ...