2.3K views · 42 reactions | Before someone is diagnosed with Fragile X syndrome, all of the signs are there, but it can take a while to see Fragile X. If your child has unexplained developmental delays, ask about a simple blood test to confirm or rule out Fragile X. Because it is a genetic disorder, knowing is important not only to your child but to past and future generations. Learn more about testing at https://hubs.ly/H0t1Bmj0. | The National Fragile X Foundation | Facebook
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2.3K views · 42 reactions | Before someone is diagnosed with Fragile X syndrome, all of the signs are there, but it can take a while to see Fragile X. If your child has unexplained
The National Fragile X Foundation. . Before someone is diagnosed with Fragile X syndrome, all of the signs are there, but it can take a while to see Fragile X. If your child has unexplained developmental delays, ask about a simple blood test to confirm or rule out Fragile X. Because it is a genetic disorder, knowing is important not only to ...
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Meet Scott Lorigan, an all-around great guy 🤹‍♂️ and a Fragile X premutation carrier. Scott recently sat down with Drs. David Hessl and Randi Hagerman to discuss his experience as a premutation carrier, his FXTAS diagnosis, the importance of clinical research, and ... your participation in the International Fragile X Premutation Registry. Who can join? Fragile X premutation carriers and relatives without a Fragile X premutation. Our efforts to advance treatment research ensures that valuable cl
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2K views · 38 reactions | FXTAS is often initially misdiagnosed as Parkinson's Disease, Alzheimer's, or a stroke. Thanks to Kelly C., a Fragile X mom and daughter of a FXTAS patient, for delivering today's fact. #FragileX https://hubs.ly/H0RBH3X0 | The National Fragile X Foundation | Facebook
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