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U.S. authorizes rapid blood test for fragile X syndrome

Posted on April 8, 2020

Originally published April 8, 2020 by Spectrum
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A photo of the X chromosome mutation underlying fragile X syndrome
A new blood test identifies the X chromosome mutation underlying fragile X syndrome. (Christine Harrison / Science Photo Library)

A new blood test can identify within seven hours whether a person carries the genetic mutation underlying fragile X syndrome, one of the leading genetic markers of autism. Previously, it could take as long as two weeks to receive the results of a blood test for fragile X syndrome. The new test is intended to be used in conjunction with family history and behavioral observation and cannot be used on fetuses.

Read the full story from Spectrum here.

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This entry was posted in News, Outside CDS and tagged Autism, diagnosis.

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