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Saint Mary's Hospital Manchester Center for Genomic MedicineInformation for Patients inheritance of the Fragile X gene Introduction This leaflet describes the way the Fragile X (Fax) gene is passed
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How to fill out screening for fragile x
How to fill out screening for fragile x
01
Contact your healthcare provider to schedule a fragile X screening test.
02
Arrive at the appointment prepared with any necessary paperwork or information.
03
Follow the instructions given to you by your healthcare provider for the screening process.
04
Be open and honest with your healthcare provider about any concerns or questions you may have about the screening.
Who needs screening for fragile x?
01
Individuals with a family history of fragile X syndrome or related disorders.
02
Individuals showing symptoms of developmental delay, intellectual disability, or autism spectrum disorder.
03
Pregnant women with a family history of fragile X syndrome.
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What is screening for fragile x?
Screening for fragile x is a test that looks for changes in the FMR1 gene, which is responsible for causing fragile X syndrome.
Who is required to file screening for fragile x?
Parents with a family history of fragile X syndrome or individuals showing symptoms of the syndrome may be required to undergo screening for fragile x.
How to fill out screening for fragile x?
Screening for fragile x usually involves providing a blood sample, which is then tested for alterations in the FMR1 gene.
What is the purpose of screening for fragile x?
The purpose of screening for fragile x is to identify individuals who may carry the gene mutation associated with fragile X syndrome.
What information must be reported on screening for fragile x?
The screening results, genetic information, and any relevant family history must be reported on screening for fragile x.
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