12K views · 396 reactions | Angelman syndrome is a rare genetic...

Angelman syndrome is a rare neurodevelopmental disorder caused by the loss of a gene called UBE3A on the mother’s copy of chromosome 15. It affects people of all races and ethnicities and often appears in infancy through feeding difficulties, delayed motor skills, and limited speech development. Individuals with Angelman syndrome experience complex challenges, including seizures and sleep disruptions, yet many also show a deep connection with those around them - smiling, laughing and maintaining

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