Comprehensive Reproductive Screen with FMR1 Repeat Expansion is an advanced genetic screening test that assesses an individual's risk of passing inherited genetic disorders to their children. It includes carrier screening for multiple genetic conditions and analyzes the FMR1 gene for repeat expansions associated with Fragile X syndrome, a common inherited cause of intellectual disability. The test helps identify individuals or couples who may have an increased risk of having a child with certain genetic conditions. Healthcare providers use the results to support reproductive planning, genetic counseling, and informed family-building decisions.
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