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ProtocolOffering fragile X syndrome carrier screening: a prospective mixed methods observational study comparing carrier screening of pregnant and nonpregnant women in the general population M Martin,1
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Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment.
Healthcare providers and genetic counselors are typically responsible for diagnosing and providing treatment for individuals with Fragile X syndrome. Parents or caregivers may also be involved in the care and management of the condition.
Offering information on Fragile X syndrome can be filled out by healthcare professionals who have experience and knowledge in diagnosing and treating genetic conditions.
The purpose of offering information on Fragile X syndrome is to educate individuals and families about the condition, its symptoms, treatment options, and available support services.
Information that may be reported on offering information about Fragile X syndrome includes genetic testing results, symptoms experienced by the individual, treatment plans, and resources for support and education.
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