This time last year Toby could only say 5 words.Due to his rare genetic disorder called Syngap1
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This time last year Toby could only say 5 words.Due to his rare genetic disorder called Syngap1
844 views1 week ago
YouTubeThe Trouble With Toby
CURE SYNGAP1 | SYNGAP1 Stories Episode 41 Short
1:06
CURE SYNGAP1 | SYNGAP1 Stories Episode 41 Short
12 views1 month ago
YouTubeCURE SYNGAP1, 501(c)(3) fka SynGAP Rese…
Kai, age 6, has SYNGAP1-related disorder. #RareDisease research helps families like his get support.
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Kai, age 6, has SYNGAP1-related disorder. #RareDisease research helps families like his get support.
1K viewsMar 3, 2025
YouTubeKennedy Krieger Institute
🐁🔬🧬SYNGAP1 gene's role in cognitive function #neuroscience #genetics #cognitivefunction
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🐁🔬🧬SYNGAP1 gene's role in cognitive function #neuroscience #genetics #cognitivefunction
2.1K viewsFeb 17, 2025
YouTubeScience X
A Night of Impact for Cure SYNGAP1 💙 My nephew Greyson was diagnosed with SYNGAP1 at just 20 months old, and it has forever changed our family’s lives. SYNGAP1 is caused by a mutation on the SYNGAP1 gene, leading to a lack of SYNGAP protein, which is essential for proper brain function. This night meant so much to us as we came together to raise money and awareness in hopes of finding a cure. A cure for Greyson would mean the world to our family. It would allow us deeper into his world and help
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A Night of Impact for Cure SYNGAP1 💙 My nephew Greyson was diagnosed with SYNGAP1 at just 20 months old, and it has forever changed our family’s lives. SYNGAP1 is caused by a mutation on the SYNGAP1 gene, leading to a lack of SYNGAP protein, which is essential for proper brain function. This night meant so much to us as we came together to raise money and awareness in hopes of finding a cure. A cure for Greyson would mean the world to our family. It would allow us deeper into his world and help
136 views3 weeks ago
TikToknichole_row3
Toby has a rare genetic disorder called Syngap1 that comes with severe behavioural issues
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Toby has a rare genetic disorder called Syngap1 that comes with severe behavioural issues
15 views1 month ago
YouTubeThe Trouble With Toby
CURE SYNGAP1 | SYNGAP1 Stories Episode 39 & 40 Short
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CURE SYNGAP1 | SYNGAP1 Stories Episode 39 & 40 Short
32 views3 months ago
YouTubeCURE SYNGAP1, 501(c)(3) fka SynGAP Rese…
2:55
#syngap1 #raredisease #nonverbalautism #epilepsy #specialneeds
6.9K views1 month ago
TikTokmisko_syngap1
2:06
SRF | Why Attend CURE SYNGAP1 Conference, SYNGAP1 Stories Ep 038 Clip
307 views8 months ago
YouTubeCURE SYNGAP1, 501(c)(3) fka SynGAP Rese…
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CURE SYNGAP1 | SYNGAP1 Stories Episode 38 Short
29 views4 months ago
YouTubeCURE SYNGAP1, 501(c)(3) fka SynGAP Rese…
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SYNGAP1 razvojna i epileptička encefalopatija 2026
85 views1 month ago
YouTubeDravet Hr
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Can you help Olly get to Mexico? Olly, from the UK, has Syngap1, the same genetic disorder as Toby.
1.4K views1 month ago
YouTubeThe Trouble With Toby
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Zeen Mobility Device on Instagram: "🎉 Zeen User of the Month: Kyle 🌟 Kyle is an inspirational young man who is living with rare genetic condition called SYNGAP1. With the Zeen’s secure seatbelt, upright support, and built-in fall protection, Kyle is empowered to safely practice walking, build strength in his legs, and move more freely throughout his home and community. “If it wasn’t for the Zeen keeping him safe,” his mom Kelli shares, “Kyle would not be able to practice independent mobility.”
107.2K views8 months ago
Instagramgo_zeen
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neuveriteľné #syngap1 #nonverbal #specialneeds #autismawareness #epilepsy
12.6K views6 months ago
TikTokmisko_syngap1
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We met up with another Syngap1 family Carmen & Stelian from Romania have been following Toby's story
3.7K views4 months ago
YouTubeThe Trouble With Toby
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autisti majú veľmi radi hračky, ktoré sa krútia #syngap1 #autismawareness #spinning #activitycube #toy
3.7K views6 months ago
TikTokmisko_syngap1
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CURE SYNGAP1 | Giving Tuesday 2025 Video Montage
95 views7 months ago
YouTubeCURE SYNGAP1, 501(c)(3) fka SynGAP Rese…
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El diagnóstico llega, pero la respuesta la construimos juntos. ❤️ En este video recorremos los años en que conocimos a quienes hoy forman parte de nuestra familia Syngap1. Cada uno llegó en un momento diferente, con miedos e incertidumbres, buscando una mano que los sostuviera y un camino a seguir. Sabemos que recibir el nombre de una enfermedad poco frecuente es abrumador, pero acercarte a una organización de pacientes es pasar de la soledad a la red. Es encontrar a otros que ya caminaron lo qu
1K views4 months ago
TikToksyngap1.argentina
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SRF | SYNGAP1 Stories Episode 37 Short
58 views10 months ago
YouTubeCURE SYNGAP1, 501(c)(3) fka SynGAP Rese…
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SRF | Cure SYNGAP1 Conference - Don't Miss Out!
170 views10 months ago
YouTubeCURE SYNGAP1, 501(c)(3) fka SynGAP Rese…
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