If you recently received a diagnosis of Angelman syndrome, the ASF and our network of Angelman families are here for you at every step of your journey. Complete the ASF Contact Registry to receive information and get connected. More info here: www.angelman.org/for-parents/newly-diagnosed | Angelman Syndrome Foundation

Children with Angelman syndrome commonly present with delayed motor milestones, gait variability, and challenges with coordination due to differences involving the UBE3A gene and downstream neuro-cerebellar pathways. These factors can influence how their bodies organise movement and respond to new motor tasks. By working collaboratively and intentionally scaffolding Van’s sensory motor system, we help his brain form new pathways while keeping the experience playful and safe. Cat offered bubbles

Therapeutic Strategies for the Treatment of Angelman syndrome Dr Allyson Berent 2020 FAST Science

Imagine a world where a one-time treatment leads to a lifetime effect – a CURE for AS. New Angelman Syndrome Foundation-funded research by Dr. Mark Zylka at UNC-Chapel Hill is pursuing exactly that by utilizing Crispr/CAS9 technology! Watch how in the video below and learn more about all ASF-funded research at www.angelman.org/research. | Angelman Syndrome Foundation