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Fragile X Syndrome (FMR1) Clinical background and genetics Contact details: Bristol Genetics Laboratory Pathology Sciences South mead Hospital Bristol, BS10 5NB Inquiries: 0117 414 6168 FAX: 0117
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Fragile X syndrome service is a program aimed at providing support and resources for individuals and families affected by Fragile X syndrome, a genetic condition that causes developmental delays and cognitive impairment.
Any individual or family member who has been diagnosed with Fragile X syndrome or who is a caregiver for someone with Fragile X syndrome may be required to file for Fragile X syndrome service.
To fill out the Fragile X syndrome service, you may need to provide information about the individual with Fragile X syndrome, their medical history, and any additional support or resources they may need.
The purpose of Fragile X syndrome service is to ensure that individuals and families affected by Fragile X syndrome have access to the necessary support and resources to help them manage the challenges of the condition.
Information that must be reported on Fragile X syndrome service may include medical history, current symptoms, treatment plans, and any additional needs or accommodations required.
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