Articles on Newborn screening

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Spinal muscular atrophy is a rare, progressive genetic disorder affecting muscle function. In France, screening is now available for all newborns. Rawpixel.com/Shutterstock (no reuse)

A camera combined with AI could help further diagnosis of movement disorders like spinal muscular atrophy in newborns

Detecting impaired motor function in infants using AI-driven motion capture is producing promising results. A French research team introduces the new screening tool for spinal muscular atrophy (SMA).
Cytomegalovirus belongs to the same virus family, Herpesviridae, as cold sores and chickenpox. Callista Images/Image Source via Getty Images

Cytomegalovirus lies dormant in most US adults and is the leading infectious cause of birth defects, but few have heard of it

Although testing for CMV during pregnancy isn’t routine and there isn’t universal screening for infants, there are steps pregnant people can take to protect themselves and their newborns.
Every child born in the U.S. has a blood sample taken to screen for genetic diseases. Helen Sushitskaya/Shutterstock.com

Sequencing the genome of newborns in the US: Are we ready?

What happens when babies are born critically ill and the doctors have no idea what is wrong? Some argue that a controversial tool called whole genome sequencing may help find the cause.
Current methods of examining newborn babies’ hearts in the first days of life are not particularly effective. jeremysalmon/Flickr

How a simple test could save babies from dying of heart disease

More babies die from undiagnosed congenital heart defects than from any other abnormality. But a simple test which is safe, painless and takes only a couple of minutes could help identify these babies…

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