The Baker Gordon Syndrome Foundation

The Baker-Gordon Syndrome Foundation was founded to help families affected by this syndrome make connections with one another. Baker-Gordon Syndrome (BAGOS), also known as, SYT1-associated neurodevelopmental disorder (SYT1 Syndrome) is a rare genetic disorder caused by mutations in the Synaptotagmin-1 (SYT1) gene. SYT1 is a vital protein that regulates the triggering of neurotransmitter release at the synapse. The mutation of the SYT1 in patients commonly causes intellectual disabilities, visual abnormalities, low muscle tone and more.

Through connecting we can support each other and explore research leading to treatments. Together, with medical professionals, we’ll discover and maximize our loved one’s potential.