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REGISTRATION FORM Name: Address: Email: Phone: Registrations will be confirmed by emailAttendee(s) please check all that apply Irish Fragile X Society Family Member CBA OT SLT SNA GP PhD Teacher Other
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Start by obtaining the necessary medical history, including information about the patient's family history and any symptoms or developmental delays observed.
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Perform genetic testing to confirm the presence of fragile X syndrome. This usually involves analyzing a blood sample or using a cheek swab to collect cells.
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Fragile X syndrome is a genetic disorder that primarily affects males. Therefore, individuals who have a family history of fragile X syndrome or those with a known genetic mutation in the FMR1 gene are at risk of needing fragile X syndrome testing.
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What is fragile x syndrome?
Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment.
Who is required to file fragile x syndrome?
Families with individuals who have been diagnosed with Fragile X syndrome are required to provide information and updates to medical professionals.
How to fill out fragile x syndrome?
Fill out information related to the individual diagnosed with Fragile X syndrome, including medical history, symptoms, and treatments.
What is the purpose of fragile x syndrome?
The purpose of Fragile X syndrome reporting is to track and monitor the progress of individuals with the condition for research and treatment purposes.
What information must be reported on fragile x syndrome?
Information such as medical history, symptoms, treatments, and any changes in condition must be reported on Fragile X syndrome.
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