SHINE Syndrome Foundation Inc

DLG4-related Synaptopathy | DLG4 SHINE Foundation

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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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.

Birth Defects, Genetic Diseases
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