Cure CAGS: What is Chopra-Amiel-Gordon Syndrome?
Chopra-Amiel-Gordon Syndrome (CAGS), also known as ANKRD17-related neurodevelopmental syndrome, is a rare genetic condition characterized by developmental delays, intellectual disabilities, and various neurological and physical symptoms.
Download and share the Gene Reviews PDF with your healthcare providers.
Resources:
The Partnership Between Rare Disease Families and Researchers: Jennifer Wells and Dr. Maya Chopra
Demystifying Genetics with Dr. Maya Chopra
Locations
The Chopra-Amiel-Gordon Syndrome (CAGS) Natural History Study
Boston Children's Hospital
Natural study contact:
Raymond Belanger Deloge, MS, CGC
Raymond.belangerdeloge@childrens.harvard.edu
"Having a son with CAGS has taught me the true meaning of strength, resilience, and unconditional love. Every challenge comes with its own victories, and through his journey, we’ve discovered the beauty in embracing uniqueness and celebrating every milestone, big or small. " -Maribeth, CAGS Mom
"A child with special needs will inspire you to be a special kind of person.” – Unknown
"Thanks to the CAGS Research team and Dr. Chopra, we feel supported and hopeful in our journey towards a cure." -Jenn, CAGS Mom
Chopra-Amiel-Gordon Syndrome (CAGS) Foundation, Inc.
Dedicated to finding CAGS treatments and a cure.
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