SHINE Syndrome Foundation Inc

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DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation A page for people interested in learning more about DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation Our mission is to improve the quality of life for children and families impacted by DLG4 SHINE through supporting collaborative research among international medical professionals, nurturing a family community, and raising worldwide awareness.

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874703593

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Pleasant Grove

Address: P.O. Box 1273, Pleasant GroveWeb: Sign in to see organisation websiteFacebook: DLG4SHINEX (Twitter): DLG4SHINERevenue: 84173ICO: 874703593

DLG4-related Synaptopathy | DLG4 SHINE Foundation Learn more about this rare disease how it affects our families and how we39re helping to find treatment. REGISTER WITH DLG4 SHINE WHAT IS A REGISTRY. NEWS Supporting Families While Advancing Research to Find Treatment for DLG4 SHINE DLG4 Synaptopathy or DLG4 SHINEis an ultrarare disease caused by a genetic mutation on the 17th Chromosome. Patients living with DLG4 SHINE typically enduretroublewithSleepDisturbancesHypotoniaIntellectual DisabilitiesNeurological Disorders andEpilepsy thus the name SHINE.

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Evelyn

2. What innovative fundraising strategies could the DLG4 SHINE Foundation implement to further support research initiatives and assist families coping with the challenges of this rare disease?

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Michael

So grateful for the work the DLG4 SHINE Foundation is doing! Each step towards awareness and research is a step towards hope for families affected by this rare syndrome. πŸ’–βœ¨

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Linda

1. How can we enhance awareness and understanding of DLG4-related Synaptopathy within both the medical community and the general public to better support families affected by SHINE Syndrome?

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Matthew

I just registered with DLG4 SHINE! Let's continue to spread awareness about this important cause and support the incredible families navigating this journey! 🌟 #SHINEbright

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