About Fragile X Syndrome | Fragile X Society | UK
About Fragile X Syndrome | Fragile X Society | UK
Sep 9, 2016
fragilex.org.uk
Video: Fragile X syndrome - Video Explanation! | Osmosis | Osmosis
Video: Fragile X syndrome - Video Explanation! | Osmosis | Osmosis
Jul 30, 2024
osmosis.org
Fragile X is a group of conditions: Fragile X syndrome, Fragile X-associated tremor/ataxia syndrome (FXTAS), Fragile X-associated primary ovarian insufficiency (FXPOI), and more emerging premutation carrier issues we are just learning about and passed through generations, often unknowingly. https://hubs.ly/H0RyK0J0 | The National Fragile X Foundation
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Fragile X is a group of conditions: Fragile X syndrome, Fragile X-associated tremor/ataxia syndrome (FXTAS), Fragile X-associated primary ovarian insufficiency (FXPOI), and more emerging premutation carrier issues we are just learning about and passed through generations, often unknowingly. https://hubs.ly/H0RyK0J0 | The National Fragile X Foundation
1.6K viewsJul 5, 2021
FacebookThe National Fragile X Foundation
What Is Fragile X Syndrome?
What Is Fragile X Syndrome?
Aug 3, 2023
fraxa.org
Exciting news! We just released a new 90-second animated video that breaks down "What Is Fragile X?" 🧬 This is the first of four engaging whiteboard videos aimed at raising awareness and educating about Fragile X Syndrome, the premutation, and its associated conditions. Whether you're a self-advocate, family member, caregiver, educator, or health professional, this video is for you. Check it out and share with someone who could benefit from learning more about Fragile X. Together, we can spread
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Exciting news! We just released a new 90-second animated video that breaks down "What Is Fragile X?" 🧬 This is the first of four engaging whiteboard videos aimed at raising awareness and educating about Fragile X Syndrome, the premutation, and its associated conditions. Whether you're a self-advocate, family member, caregiver, educator, or health professional, this video is for you. Check it out and share with someone who could benefit from learning more about Fragile X. Together, we can spread
15.3K viewsMar 31, 2025
FacebookThe National Fragile X Foundation
How is Fragile X syndrome inherited is a very common question and one of the first things a newly diagnosed family asks. Let’s be clear – Fragile X is an inherited condition. With a very rare exception, when the FMR1 gene is deleted, the gene mutation came from either the individual’s father or mother. However, we all don’t talk genetics every day, so it can be a hard concept to follow. In fact – surprisingly – we still hear of doctors incorrectly stating how the gene mutation is passed down. Ad
2:01
How is Fragile X syndrome inherited is a very common question and one of the first things a newly diagnosed family asks. Let’s be clear – Fragile X is an inherited condition. With a very rare exception, when the FMR1 gene is deleted, the gene mutation came from either the individual’s father or mother. However, we all don’t talk genetics every day, so it can be a hard concept to follow. In fact – surprisingly – we still hear of doctors incorrectly stating how the gene mutation is passed down. Ad
4.5K viewsDec 11, 2019
FacebookThe National Fragile X Foundation
Meet Mack Feldman! He has Fragile X syndrome, and his parents are Abby Gaunt and Gabe Feldman. Abby and Gabe, “support the National Fragile X Foundation because they've been there every step of the way since Mack's diagnosis. They've helped connect us to other families who are living with Fragile X syndrome. They've introduced us to the work of leading Fragile X experts and they host the most incredible conference every other year.” Abby and Gabe support fellow Fragile X families by volunteering
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Meet Mack Feldman! He has Fragile X syndrome, and his parents are Abby Gaunt and Gabe Feldman. Abby and Gabe, “support the National Fragile X Foundation because they've been there every step of the way since Mack's diagnosis. They've helped connect us to other families who are living with Fragile X syndrome. They've introduced us to the work of leading Fragile X experts and they host the most incredible conference every other year.” Abby and Gabe support fellow Fragile X families by volunteering
5.2K viewsDec 28, 2021
FacebookThe National Fragile X Foundation
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Alongside Shionogi, we’re spotlighting caregivers this #FragileXAwarenessMonth, as they have unique experiences. Jessie, mother of 5 with #FragileXSyndrome, shares her experience and what she hopes the future of care looks like. https://fragilex.org/resources/webinars/caregiver-video-jessie/ #FragileXawareness #FragileX | The National Fragile X Foundation
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