Hello world. My name is Amanda, mama bear extraordinaire to a 2 year old boy with an undiagnosed syndrome. My immediate goal is to connect with people who are researching the ZNF462 gene. I would also love to hear from other parents or persons affected by a variant of this gene. My beautiful boy who is the star of this website has a variant to that gene. I will update this website as often as I can with any updates, random thoughts, or progress made in finding out more about this microscopic mystery.