Emanuel Syndrome Guidebook

Emanuel Syndrome Guidebook for families and caregivers was updated in 2022 and can be found here.

The content of this guidebook is not a substitute for medical advice and intended for informational purposes only. You should always seek professional advice for medical concerns.

This book is dedicated to all the families around the world, raising children with Emanuel syndrome.

Stephanie Rese, founder of Chromosome 22 Central, Inc.

Thank you to the many parents around the world who shared photos of their children for this guidebook.

More: Emanuel Syndrome Awareness, Facebook Group for Families and Caregivers – Emanuel Syndrome Support Group