🧬 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… 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
126 views6 months ago
FacebookKleefstra syndrome Community
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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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
133 views6 months ago
FacebookKleefstra syndrome Community
Professor Tjitske Kleefstra –Overview: The Journey of Kleefstra Syndrome
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Professor Tjitske Kleefstra –Overview: The Journey of Kleefstra Syndrome
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YouTubeIDefine
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After undergoing countless tests and procedures, it was thanks to the work of MCRI that five-year-old Olivia was finally diagnosed with Kleefstra Syndrome, an extremely rare genetic condition that affects one in 23 million people! This diagnosis has meant that Olivia can have the best possible life with tailored care, education and support. Change a life like Olivia's this Christmas. Donate to MCRI today: http://bit.ly/2ja9QQs | Murdoch Children's Research Institute - MCRI
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FacebookMurdoch Children's Research Institute - MCRI
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“My disability doesn’t hold me back,” says Paul. “I thrive my challenges.” 💪 At 21, Paul learned that he has Kleefstra syndrome, and took part in a natural history study to better define this newly recognized disorder. #RareDiseaseDay #kleefstrasyndrome | Boston Children’s Hospital
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FacebookBoston Children’s Hospital
New TN law helps families care for children with rare disease
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🎃 Halloween and Kleefstra Syndrome 💜 We know that Halloween can be a tricky time for some families affected by Kleefstra Syndrome. The noisy decorations, flashing lights, and costumes can be overwhelming for children and adults with sensory sensitivities. So, if your loved one isn’t a fan of spooky season — please know you’re not alone. 💜 We’re sending love and understanding to all KS families who may find this time challenging. And for those who enjoy the fun — we hope you have a safe, happy
245 views6 months ago
FacebookKleefstra syndrome Community
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