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Fragile X syndrome is a genetic condition caused by a mutation in the FMR1 gene.
Healthcare providers and genetic counselors are required to file fragile x syndrome forms.
Fragile X syndrome forms can be filled out by providing information about the patient's genetic history and test results.
The purpose of fragile x syndrome forms is to document and track cases of the genetic condition in order to better understand and treat it.
Information such as genetic test results, family history of fragile X syndrome, and any symptoms or developmental delays in the patient must be reported on fragile X syndrome forms.
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