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Angelman
Syndrome Chromosome
Williams
Syndrome Chromosome
Rett
Syndrome Chromosome
0:59
YouTube
Nikolay's Genetics Lessons
What is the consequence of the FMR1 gene mutation in Fragile X Syndrome?
Fragile X Syndrome (FXS) is caused by a mutation in the FMR1 gene, which is located on the X chromosome. This gene is responsible for producing the Fragile X Mental Retardation Protein (FMRP). FMRP plays a crucial role in the development of synapses, which are the connections between neurons in the brain. It is involved in regulating the ...
1.3K views
Apr 6, 2024
Fragile X Syndrome Symptoms and Diagnosis
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Top videos
0:22
Did you know that Fragile X Syndrome is the most common inherited cause of intellectual disability? It’s caused by a mutation on the X chromosome—basically, a genetic glitch that affects brain development. 🧠⚡ People with Fragile X may have learning challenges, social anxiety, and unique ways of seeing the world. But here’s the thing—they are full of heart, personality, and resilience! 💙 With the right support, they thrive. Let’s raise awareness and break the stigma! #RareDiseaseSouthAfrica #RD
Facebook
Rare Diseases South Africa
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Fragile X Syndrome ; caused by a mutation in the FMR1 gene on the X chromosome
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In honor of World Fragile X Day, we're re-sharing this 90 second animated video to help educate everyone about Fragile X - Fragile X syndrome, the Fragile X premutation, Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS), and Fragile X Primary Ovarian Insufficiency (FXPOI). #worldfragilexday #fragilexawareness | The National Fragile X Foundation
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Did you know that Fragile X Syndrome is the most common inherited cause of intellectual disability? It’s caused by a mutation on the X chromosome—basically, a genetic glitch that affects brain development. 🧠⚡ People with Fragile X may have learning challenges, social anxiety, and unique ways of seeing the world. But here’s the thing—they are full of heart, personality, and resilience! 💙 With the right support, they thrive. Let’s raise awareness and break the stigma! #RareDiseaseSouthAfrica #RD
129 views
Feb 23, 2025
Facebook
Rare Diseases South Africa NPO 120-991
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Fragile X Syndrome ; caused by a mutation in the FMR1 gene on the X chromosome
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