U.S. authorizes rapid blood test for fragile X syndrome
Originally published April 8, 2020 by Spectrum

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