Fragile X syndrome | Genetic disorders | FMR1 gene | CGG repeats | FMRP
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YouTubeBiotech Review
Fragile X syndrome | Genetic disorders | FMR1 gene | CGG repeats | FMRP
A short and precise animated video on Fragile X syndrome, an inherited genetic disorder that causes a range of developmental problems including learning disabilities and cognitive impairment 💙 LET'S CONNECT! Instagram https://www.instagram.com/biotechreview Facebook https://www.facebook.com/biotechreview1 🎬 Background Music: Invisible ...
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Dr Mahima Kak Nagpaul🔷Gynaecologist & Fertility Expert🔷Delhi on Instagram: "Share it ✅ 🎈 Fragile X syndrome is a genetic condition caused by a mutation in the FMR1 gene on the X chromosome. This mutation leads to the gene producing insufficient amounts of a protein called FMRP, which is crucial for normal neural development. 🎈 Individuals with Fragile X syndrome often experience developmental delays, learning disabilities, and cognitive impairments. The severity of these symptoms can vary wi
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Dr Mahima Kak Nagpaul🔷Gynaecologist & Fertility Expert🔷Delhi on Instagram: "Share it ✅ 🎈 Fragile X syndrome is a genetic condition caused by a mutation in the FMR1 gene on the X chromosome. This mutation leads to the gene producing insufficient amounts of a protein called FMRP, which is crucial for normal neural development. 🎈 Individuals with Fragile X syndrome often experience developmental delays, learning disabilities, and cognitive impairments. The severity of these symptoms can vary wi
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