By testing the EZH2 genes, families at risk for Weaver Syndrome to confirm the diagnosis through DNA testing. Currently diagnosis occurs as the child develops, delaying treatment until doctors can be sure a child has the disease. Earlier testing may allow for earlier treatment, helping to lessen the impact of the mutation. There may be other genes that influence Weaver Syndrome and researchers will continue to examine them, but for now, this discovery is worth celebration.
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