What is SYNGAP1 | Rare Genetic Disorder | Special Needs Day in the Life | Diagnosis after 14 years

SYNGAP1 Syndrome is a rare genetic disorder caused by a mutation of the SYNGAP1 gene on chromosome 6.  Our son just received this diagnosis, 14 years after he was born.  In this video, I share what life is like for Kyle and our family, with a diagnosis of SYNGAP1.

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