Two-Day Test Can Spot Genetic Diseases In Newborn

A new rapid method of decoding the DNA of sick newborns may help doctors diagnose genetic diseases more quickly.

Forensic scientists have identified the bodies of 11 people last to see Chilean President alive.

WASHINGTON (October 3, 2012)--A new rapid method of decoding the DNA of sick newborns may help doctors diagnose genetic diseases more quickly in their tiniest patients in roughly two days instead of weeks.

Gene-mapping currently takes so long, and is so expensive, that it's not part of routine medical care, but researchers at Children's Mercy Hospital in Kansas City, Mo., say a speedier method could shorten the anguished wait for a diagnosis for some newborns in intensive care.

They combined a faster gene-analyzing machine with a computer program that uses a baby's symptoms to zero in on the most likely culprit.

Wednesday, they reported using the faster test to help diagnose a handful of babies, and plan to begin more routine gene mapping of sick newborns by year's end.


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