🧬 Did you know… Kleefstra Syndrome is caused by a change — either a deletion or a mutation — in the EHMT1 gene, found on chromosome 9? That’s why we’re sharing 9 facts about Kleefstra Syndrome throughout November 💙 💬 How many of our 9 facts do you think you already know? Stay tuned to find out! 👀 Follow along to learn more, raise awareness, and help shine a light on the incredible people and families in our KS community. ✨ #KleefstraSyndromeUK #RareDisease #DidYouKnow #Chromosome9 #Kleefstra
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Did you know number 7! Kleefstra Syndrome is part of a small group of conditions that affect how the body “uses instructions” in our DNA. Instead of the scientific explanation, think of it like this: 📚 Our genes are a giant instruction book. ✨ For people with KS, one of those chapters works a little differently — which can affect learning, health, and development in unique ways. But just like every book has its own story, every KS journey is wonderfully individual. 💙 💬 How would you describe
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