Phelan-McDermid Syndrome

Introducing our collection dedicated to Phelan-McDermid Syndrome Awareness. This rare genetic disorder is marked by developmental delays, intellectual disabilities, and often, autism spectrum disorder, stemming from the deletion or variation of genes on the 22nd chromosome (22Q13).

We invite you to join our community in raising awareness and providing support for those impacted by Phelan-McDermid Syndrome. For more information on how you can contribute, please visit the following websites: https://pmsf.org/ and https://www.cureshank.org/