Causes of Apert Syndrome:- Apert syndrome is a rare genetic disorder caused by a mutation in the FGFR2 gene, which controls bone development.- This gene mutation disrupts the timing of bone fusion ...
SAN ANTONIO — Two years of raising a child with a rare genetic disorder has given Flor Ramirez a unique perspective. Flor is a former KENS 5 employee, and as colleagues, we have helped raise awareness ...
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