Chopra-Amiel-Gordon Syndrome (CAGS)

Chopra-Amiel-Gordon Syndrome, also known as cags, is related to ankrd17-related neurodevelopmental syndrome and arthrogryposis, distal, type 3. An important gene associated with Chopra-Amiel-Gordon Syndrome is ANKRD17 (Ankyrin Repeat Domain 17). Affiliated tissues include brain and eye, and related phenotypes are global developmental delay and delayed speech and language development