Listen to Eric and Haley Oyler share the story about their diagnostic journey, seeking answers to their child’s developmental delays, speech delays and signs of atypical autism. Ultimately, they find answers in genetic testing with the Whole Exome Sequencing (WES) test. Their child has SETBP1 disorder which is a rare neurodevelopmental disorder caused by a change in the SETBP1 gene that causes the body to produce an insufficient amount of SETBP1 protein. Hearing the news prompts the family to take action! Hear their story!!